Provide informed written consent
Able to provide written informed consent.
Be willing and able to provide written informed consent/assent for the trial
Patients must be able to provide written informed consent
Provide written informed consent
Inability to provide informed consent
Subject or subject's representative is willing and able to provide written informed consent
Patient is able and willing to provide written informed consent
Provide informed written consent
Patients or their legally authorized representative must provide written informed consent
Be willing and able to provide written informed consent for the trial
Patient must be capable, willing, and able to provide written, informed consent
Patients must be able to provide written informed consent
Provide written informed consent
Willing and able to provide written informed consent.
Patients must be able to understand and provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Able to provide informed consent, or have a legal representative able and willing to do so
COHORT 1: Be willing and able to provide written informed consent / assent for the trial
COHORT 2: Be willing and able to provide written informed consent/assent for the trial
Able to provide valid written informed consent
Able to provide informed consent prior to initiation of study
Provide written informed consent (Subject or legal representative)
Subjects must provide written informed consent to participate
Be willing and able to provide written informed consent for the trial
Able to understand the nature of this trial and provide written informed consent
Able to provide confirmed consent
Ability to provide written informed consent
Willing and able to provide written Informed Consent and comply with the requirements of the study.
Must provide written informed consent.
Able to understand the investigational nature of this study and to provide written consent to participate in it
Provide written informed consent
Able to provide written informed consent
Provide written informed consent
Patients or their legal representative must be able to provide written informed consent;
Willingness to provide informed written consent
Able and willing to provide written informed consent to participate in this study.
Patients who can provide informed consent
Patients must provide written consent
Willing and able to provide written informed consent for the study
Be willing and able to provide written informed consent for the trial
Patients unable to provide informed consent
Able and willing to provide written, signed informed consent (assent as appropriate)
DONOR: Able and willing to provide written, signed informed consent (assent as appropriate)
Participant must voluntarily agree to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Are willing and able to provide signed informed consent.
Provide written informed consent
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent for the trial
Able to understand and comply with the requirements of the study and to provide written informed consent or age appropriate assent for pediatric patients.
Be willing and able to provide written informed consent for the trial
The subject or their legal guardian be willing and able to provide written informed consent for the trial
Provide informed consent
Provide informed written consent
Patients must be able to provide written informed consent
Patient refuses or is unable to provide written informed consent
Willing and able to provide written informed consent to participate in this investigational study.
Patients must be able to provide informed consent.
Provide informed written consent
Provide informed written consent
Patients must be of appropriate mental capacities with sufficient social support so as to be able to complete required study activities (i.e. diet record, etc) and able to provide written informed consent
Ability to provide written informed consent
Patients must be able to understand and provide written informed consent
Ability to provide written informed consent
Provide informed written consent
PART I: Able to understand and provide informed consent
PART II: Able to understand and provide informed consent
Patients or their legal representatives must be able to comprehend and provide written informed consent
Be willing and able to provide written informed consent/assent for the trial.
Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
ARM I&II: Patients must be able to provide written informed consent
Must be willing and able to provide written informed consent
Provide informed written consent
The participant (or legally authorized representative, if applicable) must be willing and able to provide written informed consent for the trial
Provide informed written consent
Willing and able to provide informed consent.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Ability to provide written informed consent.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial.
Patients must provide written informed consent.
Patients must be able to provide written informed consent
Ability to understand and willing to provide informed consent
Ability to provide written informed consent for the protocol
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Provide written informed consent for the follow up protocol.
Refusal to provide written informed consent
Patients must provide informed consent
Must be able and willing to participate in all aspects of the study and provide informed consent prior to study participation.
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent/assent for the trial
Provide written informed consent
Be willing and able to provide written informed consent.
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial.
Patients must be able to provide written informed consent.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial.
Provide written informed consent
Provide informed written consent
Patient must be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
HEALTHY SUBJECT: Be willing and able to provide written informed consent/assent for the trial
Must be willing and able to provide written informed consent
Patients (female or male) must provide informed written consent and must complete all screening assessments as outlined in the protocol
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
The patient or legal guardian must provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing to provide informed written consent
Provide written informed consent
Be willing and able to provide written informed consent/assent for the study
Patients are able to understand and provide written informed consent prior to trial participation
Be willing and able to provide written informed consent/assent for the trial
Ability to understand and provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Able to provide written informed consent
Provide informed written consent
Ability to provide informed consent and adhere to the required follow-up
Patients or their legally authorized representative must provide written informed consent
Willing and able to provide informed consent
Participants must be able to provide informed consent for treatment and trial participation
Be willing and able to provide written informed consent for the trial
Able to provide informed consent and be willing to participate in study schedule and events.
Ability to provide written informed consent
Willing and able to provide written informed consent.
Must be able to provide written informed consent before any screening procedures.
Ability to understand and provide informed consent
Able to provide written informed consent for the trial
Patients must be willing and able to review, understand, and provide written consent before study enrollment
Willing and able to provide informed consent
Ability to provide signed informed consent and willing and able to comply with all study requirements
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide informed consent
Be willing and able to provide written informed consent for the trial
Able to provide informed consent and comply with all study protocols
Able to provide written informed consent.
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Willing and able to provide written informed consent for the trial
Able to provide informed consent
Competent to provide informed consent
Able to provide written informed consent
Provide written informed consent
Ability to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Adults who are unable to provide informed consent will NOT be enrolled on this study
Be willing and able to provide written informed consent/assent for the trial
Ability to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Provide informed written consent
In the judgment of the consenting professional cognitively able to provide informed consent
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Able to provide valid written informed consent.
Be willing and able to provide written consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Subjects must be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent prior to initiation of any study procedures
Be willing and able to provide written informed consent/assent for the trial
Is willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Patient or patient’s legal representative must provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Patients must provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Subjects must be able to provide written informed consent.
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial; the subject may also provide consent for future biomedical research; however, the subject may participate in the main trial without participating in future biomedical research
Be willing and able to provide written informed consent for the trial
Patients must provide written informed consent.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Ability to provide written informed consent
Willing and able to provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Able and willing to provide informed consent and to comply with the study procedures
Be willing and able to provide written informed consent/assent for the trial
Ability to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Willing and able to provide consent
Must be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Patients or their legally authorized representative must provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Provide written informed consent (or legal representative)
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Ability to provide informed consent.
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Patients must provide written informed consent prior to any screening procedures
Ability to understand and provide informed consent
Ability to understand and provide informed consent
Be willing and able to provide written informed consent/assent for the trial
The patient must provide informed consent.
Willing and able to provide written informed consent
Provide informed written consent
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide consent
Be willing and able to provide written informed consent for trial
Patients must provide informed written consent
Patients must be willing and able to review, understand, and provide written consent before study enrollment
Ability to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Patients or their legally authorized representative must provide written informed consent
Patient able and willing to provide informed consent.
Patients unable to provide informed consent.
Be willing and able to provide written informed consent/assent for the trial
Unable to provide written informed consent
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent/assent for the trial
Patients or their legally authorized representative must provide written informed consent
Ability to provide written informed consent.
Patients must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Patient able to provide written informed consent; parent or guardian of minor patient able to provide written informed consent
Patient able to provide written informed consent for the long-term follow-up gene therapy study: 2006-0676; parent or guardian of minor patient able to provide written informed consent for the long-term follow-up gene therapy study: 2006-0676
Inability to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide informed consent
Provide informed written consent
Willingness to provide informed consent to undergo pre- and post-dose biopsy
Subject must provide written informed consent and be willing and able to comply with all aspects of the protocol
Patient or legal guardian must provide written informed consent
Ability to provide written informed consent
Patients must be able to comprehend and provide written informed consent
Subject or a legal guardian is able to voluntarily provide written informed consent.
Patients must provide informed written consent
Ability to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Patient or patient’s legal representative able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Either the subject or the subject’s legal representative must be willing and able to provide written informed consent for the trial
Patients or their legally authorized representative must provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Is willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent prior to initiation of any study-related procedures
Patients must provide written informed consent
Ability to provide informed consent for participation
Provide informed written consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Patients must provide written informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Patient must be capable, willing, and able to provide written, informed consent
Be willing and able to provide written informed consent/assent for the trial
Able to provide written informed consent
Provide written informed consent for the trial
Patients or their legally authorized representative must provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Patient or patient’s legal representative, parent(s), or guardian able to provide written informed consent
Provide informed written consent
Must provide written informed consent
Patients must be willing and able to review, understand, and provide written consent before starting therapy
Able to understand and to provide voluntarily informed consent
Patients must be able to provide informed consent
Patient or patient’s legal representative, parent(s) or guardian able to provide written informed consent
Patients must be able to provide written informed consent
Subjects must be able to provide written informed consent
Ability to provide written, informed consent
Participant must provide informed consent
Patients must provide written informed consent
Provide informed written consent
Patients 18 years or older will provide written consent. A parent or legal guardian of a patient <18 years of age will provide informed consent and patients 11 to 18 years of age will provide written assent or as per participating institutional policy.
Able and willing to provide written informed consent and to comply with the study protocol
Able to provide written informed consent
Patients must agree to participate and be able to understand and provide informed consent to participate in the trial
For Phase I and II: Patients must provide written informed consent.
Ability to understand and provide informed consent
Patient must be able to provide written informed consent
Patients must be able to provide informed consent
Willing and able to comply with the study procedures and provide written informed consent to participate in the study
Patients must be willing and able to review, understand, and provide written consent before starting therapy
Ability to provide informed consent
Must be willing and able to provide written informed consent
Subjects who provide written informed consent to participate in the study
COHORTS 1 AND 2: HEALTHY VOLUNTEERS: Ability of subject to understand and provide written informed consent
Patients must be able to provide written-informed consent
Patients must be able to provide informed consent
Eligibility criteria specific to the control arm:\r\n* Participants must be willing and able to provide written informed consent/assent for the control arm of the INdividualized Screening trial of Innovative Glioblastoma Therapy (INSIGhT) trial
Willingness to provide written informed consent for the study.
Provide written informed consent prior to any study related procedure.
Provide informed written consent
Provide written informed consent to participate on the study
Ability to provide written informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
Patients must be able to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must provide written consent
Inability to provide informed consent.
Ability of patient to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent.
Provide written informed consent
Provide written informed consent
Provide written informed consent
Participant must be able to provide written Informed Consent
Participant unwilling to provide written informed consent
Patients are not able to provide written informed consent to study participation
Be willing and able to provide written informed consent
Ability to provide informed consent.
Able to understand and willing to provide written informed consent.
Ability to understand the requirements of the study, provide written informed consent.
Ability to provide written informed consent
Able to understand and provide informed consent
Patients must provide written informed consent.
Provide written informed consent
Ability to provide written informed consent
Ability to provide written informed consent and to understand and comply with the requirements of the study
Be willing and able to provide written informed consent for the trial
Able to provide written informed consent
Can provide informed consent
Able and willing to provide informed consent
Able to provide signed, written informed consent
Patient able to provide written informed consent.
Patient able to provide written informed consent for the long-term follow-up (LTFU) gene therapy study.
Provide written informed consent
Must be able to provide informed consent.
Provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Ability to provide written informed consent
Able to provide informed consent
Patients must be able to provide written informed consent
Subjects or their legal representative must be able to understand and provide written informed consent
Provide informed written consent
Willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Inability to understand or provide informed consent
Patients must be able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent for voluntary participation in the trial
Provide informed written consent
ARM A: Ability to provide informed written consent
ARM B: Ability to provide informed written consent
Ability to provide informed consent
Ability to provide informed consent
Patients must provide informed written consent
Provide written informed consent
Be willing and able to provide written informed consent for the trial
Ability to provide written informed consent
Ability to provide informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Inability to provide informed consent
Ability and willingness to provide informed consent to participate in this study
Provide informed written consent
Ability to provide informed consent
Ability to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Ability to understand and provide voluntary written informed consent
Willingness to provide informed consent
Provide written informed consent
Patients must be able to provide written informed consent
Provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent/assent for the study
Patients must provide written informed consent prior to any screening procedures
They must be able to provide informed consent
Ability to provide informed consent
Able to provide informed consent
Patients must provide verbal and written informed consent to participate in the study
Ability to provide written informed consent
Subjects or their legal representatives must be able to provide written informed consent.
Patients must provide written informed consent.
Able and willing to provide written informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Able to provide informed consent
Patient willing and able to provide written informed consent
Patients or their legal representative (if the patient is < 18 years old) must be able to read, understand and provide written informed consent to participate in the trial.
Willingness to provide written informed consent for the study.
Willing to provide written informed consent
Provide informed written consent
Ability to provide informed written consent
Patients must provide written informed consent prior to any screening procedures
Patients, or appropriate designee, must be able to provide informed consent
Patients must be able to provide written informed consent
Able and willing to provide written informed consent to participate in the study
Able and willing to provide written informed consent and to comply with the study protocol
Participant must voluntarily agree to provide written informed consent.
Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
Willing and able to provide informed consent
Patients must provide written informed consent
Be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial.
DONOR: Willing and able to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Patients must provide written informed consent
Must be willing and able to provide written informed consent
Provide written informed consent
Ability to understand and provide written informed consent
Provide written informed consent
Able to provide written informed consent and to follow protocol requirements.
Subject or Authorized Representative is unable to provide informed consent.
Ability to provide informed consent
Must be willing and able to provide written informed consent
Ability to provide informed consent
Ability and willingness to provide written informed consent, and to comply with the requirements of the protocol
Willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent for the trial
Patients or their legally authorized representative must provide written informed consent
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial; consent may be obtained by legally authorized representative (LAR) according to the protocol
Willing and able to provide informed written consent
Provide informed written consent
Patients or their legally authorized representative must provide written informed consent
Ability to provide informed consent
Patient or patient’s legal representative able to provide written informed consent
Ability and willingness to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Patients or their legally authorized representative must provide written informed consent
Able and willing to provide written informed consent
Either the subject or his/her legally authorized representative be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent and authorization permitting study-related release of personal health information
Be willing and able to provide written informed consent/assent for the trial
Able to provide informed written consent
Be willing and able to provide written informed consent for the trial
Provide written informed consent
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
All patients must be willing and capable to provide informed consent to participate in the protocol
Ability to provide written informed consent and comply with study requirements
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Ability to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Provide informed written consent
Patients, or appropriate designee, must be able to provide informed consent
Provide informed written consent
Ability to provide informed written consent
Subject is able to provide written informed consent.
Able to provide informed written consent
Adults who are unable to provide informed consent will NOT be enrolled on this study
Patients must provide informed consent
Willing and able to provide informed consent
Patient should be able to provide informed consent
Patients must provide verbal and written informed consent to participate in the study
Patients must provide written informed consent prior to any registration on study
Ability to provide written informed consent
Ability and willingness to provide written informed consent
COHORT A: The subject must be willing and able to provide informed consent
COHORT B: The subject must be willing and able to provide informed consent
Unable to provide informed consent
Ability to provide informed consent
Patient must be capable, willing, and able to provide written, informed consent
For adult patient, the patient is able to provide informed consent. For pediatric patient, a parent is able to provide informed consent.
Patient willing and able to provide written informed consent for the trial
Provide informed written consent
Provide written informed consent
Provide informed written consent
Patients must be able to provide written informed consent
Patients must be willing and able to review, understand, and provide written consent before starting therapy
Able to provide written informed consent
Provide informed written consent
Ability and willingness to provide written informed consent
Provide informed written consent
Patients must provide informed written consent
Ability to provide informed written consent
Inability to provide informed consent
Willing and able to provide informed consent
Willing and able to provide written informed consent
Able and willing to provide written informed consent.
Patients willing and able to review, understand, and provide written consent before starting therapy
Able to provide written consent
Cognitively impaired patients who cannot provide informed consent
Provide informed written consent
Patients who provide written informed consent for participation in this trial
Able to provide informed consent and follow protocol requirements.
Inability to provide informed consent.
Patients must be able to provide informed consent
Provide informed written consent
Provide written informed consent
Able to provide written, informed consent
Provide informed consent
Inability to provide informed consent
All patients must be willing and capable to provide informed consent to participate in the protocol
Patients must be willing and able to provide signed informed consent and comply with the study protocol.
Ability to provide written informed consent
Patient or guardian willing and able to provide informed consent.
Inability to provide informed consent
Ability to provide informed consent
Provide written informed consent
Ability to provide informed consent.
Be willing and able to provide written informed consent/assent for the trial
Ability to provide informed consent
Understands the potential risks and benefits of study participation and is willing to provide written informed consent.
Patients must be able to provide written informed consent
Ability to understand and provide informed consent
Able to provide informed consent for the study
Patients must be able to provide informed consent
Patients must provide written informed consent
Willing and able to provide written Informed Consent and adhere to study procedures.
Patients must be willing and able to review, understand, and provide written consent before starting therapy
Inability to provide informed consent
Provide informed written consent
Patients must provide informed consent
Patients or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial
Provide informed written consent
Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
Be willing and able to provide written informed consent/assent for the trial
Willingness to provide written informed consent for the study.
Patients must be able to provide written informed consent
Willing and able to provide informed consent
Provide written informed consent.
Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
Willing and able to provide written informed consent
Provide informed written consent
Patients unable to provide informed consent
Able to provide written informed consent.
Patients, or appropriate designee, must be able to provide informed consent
At least 18 years of age and willing and able to provide informed consent.
Ability to provide written informed consent
Willing and able to provide informed consent
Able to understand and have the ability to provide written consent
Patients must provide written informed consent.
Willingness and ability to provide written informed consent and to comply with the protocol requirements
Able to provide informed consent
Able to provide written informed consent and to follow protocol requirements
Patient, or his/her legally authorized representative, is able to understand and provide informed consent.
Willing and able to provide written informed consent.
Provide written informed consent prior to any screening procedures
Patients or their legally authorized representative must provide written informed consent
Ability to understand and provide informed consent
Ability to provide informed consent
Inability to provide informed consent
Provide written informed consent prior to any screening procedures
Subject is able to voluntarily provide written informed consent.
Provide informed written consent
Subjects between 12 and 35 years of age, inclusive, at the time of consent/assent, and able to provide written consent/assent, if applicable.
Willing and able to provide written informed consent
Provide written informed consent
Must be willing and able to provide written informed consent and comply with the protocol and study procedures
Provide informed written consent
Ability to provide informed consent
Ability to provide informed written consent
Able to provide informed consent, child assent with parental consent or surrogate consent when applicable
4. Patient is able and willing to provide written informed consent to participate in the study.
Ability to provide written informed consent
Patients must be able to provide written informed consent
Subject or subject's representative is willing and able to provide written informed consent
Willing and able to provide informed consent;
Provide informed written consent
Ability to provide informed consent
Provide informed written consent
Provide written informed consent
Inability to provide informed consent
Able to provide written informed consent
Provide written informed consent and willing to comply with protocol requirements.
Ability to understand and provide written informed consent to participate in this study.
Willing and able to provide written informed consent.
Inability to provide adequate informed consent
Able to understand and provide written informed consent
Patients must be able to provide informed consent
Ability to provide written informed consent
Willing and able to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Provide informed written consent
Patients must provide written informed consent
Provide informed written consent
Age 18 years or older and willing and able to provide informed consent;
Have ability to provide full written consent
Able to understand and provide written informed consent
Patients or their legally authorized representative must provide written informed consent
Ability to provide informed written consent
Able to provide written informed consent, and agree to practicing 2 forms of birth control during the study
Provide informed written consent
Provide written informed consent
Provide informed written consent
Be able to provide written informed consent
Both must provide informed consent
Able to provide informed consent
Unable to provide consent
Able to read either English or Spanish and able to provide written (via paper), verbal consent or on-line informed consent
Able to provide written informed consent
Be able to provide informed consent
Patient/caregiver can provide informed consent
Patient/partner is able to provide informed consent
Able to comprehend and provide informed consent
Able to provide informed consent
Patient able to provide his/her own written informed consent and speak English
Inability to provide informed consent
Unable to provide informed consent
Patients must provide written informed consent prior to any screening procedures
Able to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Patients unable to understand the research protocol and/or provide informed consent
The ability to provide informed consent
PATIENT & PARTNER: Able to provide informed consent
Provide written informed consent
Able to provide informed consent
Are able to provide voluntary, written consent
Inability to provide a fully informed consent.
Must be able to provide own consent
PATIENTS AND CAREGIVERS: Able to provide informed consent.
Able to provide informed consent
PROVIDER ELIGIBILITY: The participant is willing to provide informed consent in English
Unwilling to provide informed consent
Phase I: Able to provide informed consent
Phase II: Able to provide informed consent
Patients who are unable to provide informed consent in English will be excluded
Able to provide informed consent
Cannot provide meaningful informed consent
Patients unable to provide informed consent
Ability to provide informed consent
In the judgment of the consenting professional cognitively able to provide informed consent
In the judgment of the consenting professional cognitively able to provide informed consent
Able and willing to provide informed consent
PATIENTS AND PARTNERS: Able to provide consent
Ability to provide informed consent
Adults who are able to provide informed consent
Willing and able to provide informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Can provide informed consent (e.g., no cognitive impairment)
CAREGIVER: Can provide Informed consent
Must provide written informed consent
Psychiatric disorder which would render the subject unable to provide informed consent
Subject is willing to provide written informed consent
Patient or patient’s legal representative(s) is/are able to provide written informed consent to participate
Ability to provide informed written consent
Unable to provide informed consent
Subject is able to provide informed consent
Are unable to provide informed consent
Ability and Willingness to provide informed consent
Unwilling to provide informed consent
Able to provide informed consent
Be willing to provide written informed consent to participate in the study which includes several clinical evaluations, provide access to medical records/primary care physician (PCP), and allow all interviews and PSST therapy sessions to be audiotaped.
Provide written informed consent
Capable and willing to provide Informed consent
FCGs: Able to provide informed consent
PATIENTS: Not able to provide informed consent
Able to provide informed consent
Able and willing to provide written consent
Patients unable to provide informed consent
Patients must be able to provide written informed consent
Willing and able to provide informed consent
Not willing and able to provide informed consent
Patients must be able to provide informed consent
Provide written informed consent
Provide written informed consent prior to screening
Be able to provide written informed consent
Able to provide informed consent
Willing to provide informed written consent
PHASE I: Able to provide meaningful informed consent
PHASE II: Able to provide meaningful informed consent
Ability to provide informed written consent
Inability to provide informed consent
Inability to provide informed consent
Willing and able to provide signed, informed consent
Willing and able to provide written informed consent
Subjects able to provide informed consent
Able to provide written informed consent and authorization for release of health information
Able and willing to provide consent (both)
Ability to provide informed consent
Able to provide written informed consent
Inability to provide informed assent/permission/consent
Ability to provide informed written consent
Can provide informed consent
Ability to provide informed written consent
Inability to provide informed consent
PATIENT: Be able and willing to provide informed consent
Unable to provide informed consent
Able and willing to provide informed consent
Provide informed written consent
Patients must be willing and able to review, understand, and provide written consent
Ability to provide written informed consent
Patients willing and able to review, understand, and provide written consent
Provide informed written consent
Unwilling to provide informed consent
Unwilling to provide informed consent
Patients willing and able to review, understand, and provide written consent before starting therapy
Unwilling to provide informed consent
Patients who are willing and able to review, understand, and provide written consent
Willing and able to provide, signed informed consent
Provide informed written consent
Able to provide informed consent
Inability to provide informed consent
The subject must be willing and able to provide informed consent
Able to provide informed consent
Patients must provide written informed consent prior to any screening procedures
Patients must provide written informed consent to participate in the study
Able to provide informed consent
Cognitively able and willing to provide consent
Provide informed written consent
Patients must be willing and able to provide a written informed consent
Unable to provide informed consent
Able and willing to provide written informed consent
Provide informed consent
Patients who cannot provide a valid consent
Subjects unable to provide consent
Patients can provide informed consent
Be able to provide informed consent in English or Spanish
Able to provide informed consent in English
Unable to provide informed consent
CONTROL (HEALTHY) GROUP: Unable to provide informed consent
Participant is unable to provide informed consent
Ability to provide informed written consent
Unable to provide informed consent
Inability to provide informed consent
Willing to provide informed consent/assent for study participation
Willing to provide informed consent/assent for study participation
Unable to provide informed consent
Subjects willing and able to provide consent to participating in the study
Able to provide verbal consent
Able to provide informed consent
Patients must be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Ability to read and provide written informed consent
Willingness to provide written informed consent
Provide written informed consent.
Able to provide informed consent to participate in the study
Unable to provide informed consent
Able to understand and willing to provide informed consent for the RPFNA’s and study participation
Unable to provide informed consent
Inability to provide informed consent
Able to provide informed consent
Have the ability to provide informed consent in English
FOLLOW UP ASSESSMENTS: Have the ability to provide informed consent in English
Patients must be able to provide written informed consent
Ability to provide written informed consent
Inability to provide informed consent
Able to provide informed consent
Understand the study procedures and able to provide informed consent
Patients who are willing and capable to provide informed consent
Able and willing (or have legal representative) to understand the study and provide consent
Inability to provide informed consent (and assent, if subject is under the age of 18)
the ability to comply with the study protocol and provide informed consent
Capable and willing to provide informed consent
Patient must be able and willing to provide written informed consent
The patient is willing and able to provide informed consent.
Patients unable to provide informed consent
Be willing and able to provide written informed consent/assent for the trial
Able to provide legally effective informed consent
Provide written informed consent for the study
Are able to provide informed consent
Are unable to provide informed consent
Patients must be able to provide written informed consent
Able to provide written informed consent and willing to comply with protocol requirements
Able to provide written consent
Patients must be capable and willing to provide informed consent
Inability to provide informed consent on their own behalf
Unable to provide written consent
Willingness to participate in the study and able to provide informed consent
Patients must be able to provide informed consent
Able to provide written consent
Patients must be capable and willing to provide informed consent.
Able to provide informed consent and follow the study guidelines
Patient able and willing to provide informed consent
Patient is able to provide written informed consent prior to study registration
Patients must be able to provide written informed consent
Cannot provide written informed consent
Patients must be able to provide written informed consent
Cannot provide written informed consent
Ability to provide informed consent
Able to provide informed consent
Able to provide written informed consent
Able to provide written consent
Able to provide written consent
Unable to provide informed consent
Subject/legal representative willing and able to provide written informed consent
Able to provide informed consent
Provide informed written consent if >= 18 years; if < 18 years, provide informed written assent and parent or legal guardian provide informed written consent
Provide written informed consent
Refusal to provide informed consent
Patients must provide written informed consent
Females unable to provide informed consent
Subjects unable to provide own consent are not eligible
Subject and/or guardian is able to provide written informed consent prior to study registration
Able to read or understand and provide informed consent
Patient and/or guardian is able to provide written informed consent prior to study registration
Patient and/or guardian is able to provide written informed consent prior to study registration
Patient and/or guardian is able to provide written informed consent prior to study registration
Able to provide written informed consent
Patients must be able to provide written informed consent
Cannot provide written informed consent
Able to provide written informed consent.
Ability to provide informed consent
Inability to provide informed consent
HEALTHY VOLUNTEERS: Patient is willing to provide informed consent
HCC PATIENTS: Patient is willing to provide informed consent
Able to provide written consent
Able to provide written informed consent
Inability to provide written informed consent
Participant willing to provide a written informed consent
Willing and able to provide written informed consent
Patient and/or legal guardian able and willing to provide informed consent
Patient unable to provide informed consent
Patients must be able to provide written informed consent
Those who are pregnant, claustrophobic, or unable to provide informed consent
Are able to provide informed consent
Are unable to provide informed consent
Ability to provide written informed consent
Subjects unable to provide own consent are not eligible
Unable to provide informed consent
Able to provide informed consent
Ability to provide informed consent
Inability to provide informed consent
Unable to provide consent
Patient and/or guardian is able to provide written informed consent prior to study registration
Subjects must to able to provide informed written consent prior to study entry
Provide informed written consent
Patients must provide informed written consent
Willing and able to provide informed written consent
Be willing and able to provide written informed consent for the trial
Patients must provide written informed consent
The patient must be willing and able to provide informed consent
Patients must be able to provide written informed consent
Cannot provide written informed consent
Willing and able to provide a written informed consent
Must be able to provide a written informed consent
Inability to provide informed consent
Unable to provide informed consent
Patients unable to provide informed consent
Ability to provide written, informed consent.
Able to provide written informed consent
Able to provide written informed consent and willing to comply with protocol requirements
Willing and able to provide informed consent
Are able to provide informed consent
Are unable to provide informed consent
Unable to provide informed consent
Be willing and able to provide informed consent
NORMAL VOLUNTEERS: Be willing and able to provide informed consent
Provide written informed consent and willing to comply with protocol requirement
Able to provide informed consent
Able to understand the experimental nature of the study and provide informed consent
Provide informed written consent
Willing and able to provide written informed consent
Subjects are required to be willing and able to provide written informed consent
Participants who are not able to understand or provide written informed consent
Ability to provide informed consent
Ability to provide written informed consent obtained prior to participation in the study
Able to provide informed consent
Ability to provide consent
PATIENTS: The ability to provide informed consent
Able to provide informed consent to participate in the study
Must be able to provide informed consent
Willing and able to provide informed consent and fill out demographic, disease, and pain assessment questionnaires
Can provide informed consent
Be willing and able to provide written informed consent.
Patients unable to provide informed consent
Men who are unable to provide their own informed consent
Patients must be able and willing to provide written informed consent prior to any study related procedure.
Able to provide written informed consent.
Ability and willingness to provide written informed consent
Able to provide written informed consent
Be willing and able to provide written informed consent/assent for the trial
Participants must voluntarily agree to provide written informed consent.
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial
Be willing and able to provide written informed consent/assent for the trial