--- a
+++ b/clusters/3009knumclusters/clust_144.txt
@@ -0,0 +1,677 @@
+Patients or their legal representatives must be able to read, understand, provide and sign informed consent to participate in the trial
+Willing to sign Informed Consent;
+Subjects must be willing and able to sign the informed consent and comply with the study protocol.
+Able to agree to and sign informed consent and to comply with the protocol
+The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines; assent, when appropriate, will be obtained according to institutional guidelines
+Willing and able to give written informed consent.
+Able to understand and sign an informed consent (or have a legal representative who is able to do so)
+Able to give a written informed consent.
+Able and willing to give informed consent
+Patients must be able to give adequate informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to give informed consent
+Able and willing to give valid written informed consent.
+Must be able to understand and voluntarily sign an informed consent form (ICF).
+Subjects must voluntarily sign an informed consent form (ICF); and able to meet all study requirements
+Inability to understand and sign informed consent
+Willing and able to comply with the protocol and sign informed consent
+Patients and donors must be able to sign consent forms (or if a minor the parent will sign); donors should be willing to donate
+Participant must be aware of the nature of her malignancy, understand the study requirements and risks and be able and willing to sign a written informed consent document
+Competent to sign informed consent
+Able to understand and voluntarily sign an informed consent form
+Subject must be able to understand and be willing to sign a written informed consent document
+Participant is able to understand and comply with study requirements and is willing to sign a written informed consent document
+PIK3CA WILD TYPE COHORT (closed 03/17/2016): Able to understand and willing to sign an IRB-approved written informed consent document
+Patient able to understand, sign, and date the written informed consent form at screening visit prior to any protocol-specific procedures
+PROCUREMENT: Patient able to give informed consent
+TREATMENT: Patient able to give informed consent
+Patient, parent/guardian able to give informed consent
+Patient, parent, or legal guardian must be able to understand and be willing to provide informed consent
+Willing and able to understand and sign an informed consent inform and to comply with all aspects of the protocol.
+All subjects must be able to comprehend and sign a written informed consent document
+INCLUSION CRITERIA FOR REGISTRATION (HER2 MUTATION IDENTIFIED BY WASH U GPS LABORATORY): Able to understand and willing to sign an IRB approved written informed consent document
+INCLUSION CRITERIA FOR REGISTRATION (HER2 MUTATION IDENTIFIED AT AN OUTSIDE CLIA CERTIFIED LOCATION): Able to understand and willing to sign an IRB approved written informed consent document
+Willing and able to comply with the study procedure and sign a written informed consent
+In the haplo cohort, the donor and/or legal guardian must be able to sign informed consent documents.
+Able to sign an informed consent
+Patients must be able to give informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure; subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other study requirements
+Sign (or their legally-acceptable representatives must sign) an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study
+Sign informed consent.
+Patients or their legal representative must be able to read, understand and sign an informed consent
+Must be able to understand and voluntarily sign an informed consent form (ICF).
+Willing and able to give written, and dated, informed consent
+Able to understand and voluntarily sign the informed consent form, and able to comply with the study visit schedule and other protocol requirements; written informed consent obtained prior to any screening procedures
+ARM 2 - A: Able to understand and willing to sign an IRB-approved written informed consent document
+Able to understand and willing to sign written informed consent.
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Subject is willing and able to give prior written informed consent for investigation participation; and
+The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document, inclusive of assent where appropriate, according to institutional guidelines
+INCLUSION CRITERIA FOR STRATUM C: The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document, inclusive of assent where appropriate, according to institutional guidelines
+Patients who are able to give informed consent
+Willing and able to give written informed consent
+Patient must be able to understand and willing to sign a written informed consent document
+Willing and able to give written informed consent
+Able to give written informed consent.
+Able to understand and sign the informed consent document
+Willing and able to give informed consent
+Are able to comprehend and willing to sign an informed consent form
+Age >18 and must be able to read, understand, and sign informed consent
+Able to understand and voluntarily sign an informed consent form
+Willingness to sign the healthy volunteer informed consent form
+Understand and voluntarily sign an informed consent form
+Patients must be able to understand and sign informed consent form
+Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
+Able to understand and sign the informed consent document
+Must be able and willing to give written informed consent.
+Willing and able to sign informed consent
+Able to understand and sign the informed consent document
+Patients must be able to understand and give informed consent
+Able to understand, and willing to sign, a written informed consent document.
+Understand and voluntarily sign an informed consent form.
+Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
+Each patient must be willing to participate as a research participant and must sign an informed consent form.
+Sign an Informed Consent Form (ICF);
+Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
+All subjects must be able to comprehend and sign a written informed consent document
+Patient must be able to understand and willing to sign a written informed consent document
+Able to give informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to understand and sign the informed consent document
+Able to understand and voluntarily sign an informed consent form
+Patients must be able to provide informed consent and be willing to sign an approved consent form that conforms to federal and institutional guidelines
+Patient must be able to comprehend and sign a written informed consent and be willing to comply with all study procedures
+Patient, parent, or legal guardian must be able to understand and willing to provide informed consent
+Able to understand and voluntarily sign a written informed consent, and willing and able to comply with protocol requirements
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+All subjects must be able to comprehend and sign a written informed consent document
+Willing and able to give informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+All subjects must be able to comprehend and sign a written informed consent document
+Adult patients must be able to understand and sign a written informed consent. For pediatric patients, the parent/legal guardian or representative must be able to understand and sign a written informed consent. Assent, when appropriate, will be obtained according to institutional guidelines.
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure; subjects must be willing and able to comply with scheduled visits, treatment schedule, laboratory testing, and other study requirements
+Patients must be able to understand and be willing to give informed consent; parent or legal representative will be asked to consent for patients younger than 18 years old
+Donors must be able to give informed consent
+Willing and able to understand and voluntarily sign a written informed consent
+Able to understand and sign informed consent
+Participants must be able to understand and sign a written informed consent form and understand the importance of adherence to study treatment and protocol; in addition, participants must demonstrate a willingness to follow all study requirements, including the concomitant medication restrictions, throughout the study
+Subject can understand and sign the informed consent document, can communicate with the investigator, and can understand and comply with the requirements of the protocol.
+Understand and voluntarily sign an informed consent document
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to give informed consent
+Ability to sign informed consent
+Patients are able to understand and willing to sign the informed consent.
+Patients must be able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Patient must sign a study specific informed consent form
+Must be able to give informed consent; subjects unable to give informed consent will not be eligible for this study
+Able to sign informed consent
+Able to understand and give written informed consent
+Patients or their legal representative must be able to read, understand, and sign a written informed consent
+Understand and voluntarily sign an informed consent, and be able to comply with study procedures and follow-up examinations.
+Patient must be able to understand and willing to sign a written informed consent document
+Able to understand and willing to sign informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to understand and sign the Informed Consent Document
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+STUDY TREATMENT: Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Subject must understand risks and benefits of the protocol and be able to give informed consent
+Able to understand and sign the informed consent document
+Patient must be able to understand and willing to sign a written informed consent document
+All patients must sign a study-specific consent form
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Patients must be capable of giving informed consent and be willing and able to comply with schedule
+A legal parent/guardian or patient must be able to understand, and willing to sign, a written informed consent and assent document, as appropriate
+All subjects must be able to comprehend and sign a written informed consent document
+Able to understand and sign informed consent
+Understand and voluntarily sign an informed consent form
+Patient refuses to sign informed consent
+Able to understand and sign the informed consent document
+Able to understand and voluntarily sign a written informed consent, and willing and able to comply with protocol requirements
+Subjects who are able to understand and sign an informed consent document
+Able to give informed consent
+Patients must be able to understand and be willing to sign the written informed consent form
+Subjects must be able to give informed consent
+Able and willing to give valid written informed consent
+All subjects must be able to comprehend and sign a written informed consent document
+Patient or patient’s legal representative able to sign informed consent
+Able to understand and sign the informed consent document
+Patient must be able to understand and willing to sign a written informed consent document
+Patient or legally appropriate proxy must be able to understand study instructions and sign consent
+Able to understand and sign the informed consent document
+Patients must be willing and able to sign informed consent for themselves
+Be able to give informed consent
+Patients must be able to understand and voluntarily sign an informed consent form
+Patients must sign a study-specific consent form
+Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
+Patients must be able to understand and sign an informed consent form
+Patients must be willing to sign the protocol-specific written informed consent
+Refusal to sign the informed consent
+Refusal to sign the informed consent
+Able to understand and sign the informed consent document
+Able to understand and sign informed consent
+Understand and voluntarily sign an informed consent form
+Able to understand and willing to sign a written informed consent document
+Able to understand and willing to sign an IRB-approved written informed consent document
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to understand informed consent
+Patients must be willing and able to understand the informed consent document
+Able to give informed consent
+Refusal to sign informed consent
+Fully understand the study and voluntarily sign the informed consent form;
+Able to sign informed consent
+Patient must be able to comprehend the approved consent document and have the willingness to sign it; the patient prior to enrollment and the administration of any protocol-specific therapy must sign the consent document
+Able to sign informed consent
+Patient able to give informed consent
+All subjects must be able to comprehend and sign a written informed consent document
+All subjects must sign a written informed consent
+Able to understand and then sign an informed consent form (ICF) prior to initiation of any study-specific procedure and treatment.
+DONOR: Able to understand and sign informed consent
+Patient or legally authorized representative able to sign informed consent
+Must be able and willing to give written informed consent
+Be able to give informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form
+Able to understand, and the willingness to give, informed consent for the study
+Understand and voluntarily sign an informed consent form
+Patient able to sign informed consent
+Patient is able to understand and is willing to sign the informed consent form
+Understand and voluntarily sign an informed consent form
+PROCUREMENT: Patient able to give informed consent
+TREATMENT: Patient able to give informed consent
+Patient, legally authorized representative (LAR), or parent able to sign informed consent; able to give assent for patients age 7-17
+Must sign the picture consent form
+Able to understand, and willing to sign a written informed consent document
+Patient must be able to understand and be willing to sign a written informed consent document
+Be able and willing to give informed consent
+Patients must be able to understand and be willing to sign a written informed consent document
+Sign an informed consent document
+Sign a written informed consent form
+Patients should be willing and able to give informed consent
+Patients are willing and able to give informed consent (Phase II only)
+DONOR: Ability to comprehend and willing to sign an informed consent
+The patient is able to understand and give informed consent
+Willing and able to give written informed consent
+Patients must sign an informed consent document
+Able to understand and sign the informed consent document
+Patient or legally authorized representative able to sign informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to understand the consent competent to sign
+Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent; patients aged 7 to < 18 to provide assent
+Patients (parents/guardians for those < 18) and donors must be able to sign consent forms
+Patients must be able to understand and sign a written informed consent document and complete study-related procedures and questionnaires
+Patient or patient’s guardian is able to give informed consent
+Understand and voluntarily sign an informed consent document
+Patients must be able to understand and sign an informed consent indicating that they are aware of the investigational nature of this study in keeping with the institutional policies.
+Patients willing and able to sign consent
+Patient or legally authorized representative able to sign informed consent
+Able to understand and sign a written informed consent document.
+Patient and/or legal guardian must be able to sign informed consent.
+DONOR: Able to give informed consent
+Ability of subject to understand, and be willing to sign informed consent
+Inability to sign informed consent document
+Able and willing to give informed consent, and to undergo staging including PET scanning
+Each patient much be willing to participate as a research subject and must sign an informed consent form
+Willing and able to give written informed consent
+All subjects must sign a written informed consent
+Patients must be able to understand and be willing to sign a written informed consent document
+Patient must be able to understand and willing to sign a written informed consent document
+Willing and able to give informed consent
+Patients must have the ability able to give informed consent
+Able and willing to give informed consent.
+Understand and voluntarily sign an informed consent form
+The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
+Patients must sign informed consent prior to study entry
+Able to give informed consent
+Refusal to sign the informed consent
+Able to give informed consent
+Patient and/or responsible person able to understand and sign consent
+Patient and/or responsible person able to understand and sign consent
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Able to understand and sign a written informed consent form
+Patients must be able to understand and give informed consent
+Understand and voluntarily sign an informed consent form
+patients who are able to give informed consent
+Able to give informed consent
+Able to give informed consent
+Understand and voluntarily sign an informed consent form.
+Patients must sign informed consent
+Patient is able to give and sign study specific informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Willing and able to understand and sign the study specific Informed Consent Form
+Patients must be able to understand and sign the informed consent
+Willing and able to give informed consent
+Patients must understand and voluntarily sign an informed consent form
+Able and willing to give valid written informed consent.
+Subject must voluntarily sign and understand written informed consent.
+Able to read or understand and give informed consent.
+Patient able to understand, sign, and date the written voluntary informed consent form at screening visit prior to any protocol-specific procedures
+Must understand and voluntarily sign informed consent;
+Able to understand and sign an Informed Consent
+Able to sign informed consent
+The patient, or their representative, is able to understand the study and is willing to consent to participation in the study.
+Able and willing to give informed consent.
+Able and willing to give informed consent.
+Able to comprehend and willing to sign the informed consent form
+Patients must sign an informed consent
+Willing and able to consent for self to participate in study
+Able to give informed consent.
+Able to give informed consent
+Unable to sign informed consent
+Able to give written informed consent to participate in the study
+Subjects must be able to understand and be willing to sign a written informed consent document
+Part 1: be able to understand the description of the study and give written informed consent
+Provision to sign and date the consent form
+Able to understand and sign the informed consent document
+Willing and able to give informed consent.
+Willing and able to give informed consent.
+Sign (or their legally-acceptable representatives must sign) an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.
+Patient or legally authorized representative able to sign informed consent
+Willing and able to give informed consent
+Be able to understand and be willing to sign a written informed consent document
+Must be able and willing to give written informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Subjects must understand and sign the study specific informed consent
+Able and willing to give valid written informed consent
+The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
+Be able to understand and willing to sign an informed consent form (ICF).
+Participants must be able to understand and willing to sign a written informed consent document
+Patients must be able to understand and willing to sign a written informed consent document
+Informed consent: all subjects must be able to comprehend and sign a written informed consent document
+Subjects must freely sign informed consent to enroll in the study
+Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
+Ability of subject to understand, and be willing to sign informed consent
+Patients must be able to understand and willing to sign a written informed consent document
+Participant is willing and able to give written informed consent
+The patient must sign an informed consent form (ICF)
+Patient is willing and able to give written informed consent
+Patients must sign the informed consent document
+Participants must sign an approved informed consent form (ICF).
+Patients must be able to understand and willing to sign an informed consent
+Must sign informed consent
+Patients must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to comprehend and willing to sign an Informed Consent Form (ICF)
+Able to understand and sign the informed consent document
+Able to understand and sign informed consent
+Able to understand and sign the informed consent document
+Able to understand and sign the informed consent document
+Patients must sign study specific informed consent
+Patients must sign an informed consent
+Patients must be able to give informed consent
+Patient must be willing to sign informed consent
+Patients must be willing and able to sign informed consent
+Patients must be able to understand and sign informed consent
+Patients must be willing and able to sign informed consent
+Patients must be able to give informed consent
+Patients must be able to read and understand the informed consent document; patients must sign the informed consent indicating that they are aware of the investigational nature of this study
+Able to understand and give informed consent
+Understand and give informed consent
+Patient or legal guardian must be able to give informed consent
+Able to give informed written consent
+Able to give informed consent
+Patient must be able to understand and willing to sign an informed consent
+Willing and able to sign informed consent
+Must be willing to sign a written informed consent.
+Willing and able to sign written informed consent and be able to comply with the study protocol for the duration of the study
+Able to give a written informed consent.
+AMKL PATIENTS: Patients must be able to understand and willing to sign a written informed consent
+MF PATIENTS: Patients must be able to understand and willing to sign a written informed consent
+Able to comprehend and willing to sign an informed consent form (ICF)
+Patients must have the ability to sign an approved informed consent form (ICF).
+Able to comprehend and willing to sign informed consent form
+All patients must sign an informed consent prior to enrollment.
+Must be able and willing to give written informed consent
+Sign (or their legally-acceptable representatives must sign) an informed consent document\r\nindicating that they understand the purpose of and procedures required for the study, including\r\nbiomarkers, and are willing to participate in the study
+Able and willing to give valid written informed consent
+Patients must be able and willing to give written informed consent
+Willing and able to give informed consent and adhere to protocol therapy
+Subjects must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.
+Patients must sign a study-specific consent form
+Ability to understand and voluntarily sign an informed consent form
+Willing and able to give informed consent
+Patients must sign an informed consent document
+Voluntarily agree to participate and sign an informed consent document
+Patient must understand and voluntarily sign an informed consent, and be able to comply with study procedures and follow-up examinations
+Able to understand and willing to sign the informed consent form
+Patients must be able to understand and be willing to sign a written informed consent document.
+Subjects must be able to understand the potential risks and benefits of the study, and be able to read and give written informed consent
+Willing and able to give written informed consent.
+Patients must sign an informed consent document
+(Turnstile 1 & Turnstile 2) Willing and able to give informed consent.
+Able to understand and sign the informed consent document
+Understand and give informed consent
+Able to comprehend and willing to sign the informed consent form
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+The subject must sign and date all informed consent statements; children will sign the assent form and their guardian will sign the consent form
+Refusal to sign informed consent
+Able to understand and sign informed consent
+Subjects must be able to give informed consent
+Patients must sign informed consent
+Able to give informed consent
+Able and willing to give valid written informed consent.
+Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent; age 7-18 able to provide assent
+Patients must sign informed consent
+The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
+ELIGIBILITY FOR ENROLLMENT/SCREENING (ARMS 1 AND 2): Patients must be able to give informed consent
+Patients able to understand and willing to sign a written informed consent documents
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to understand and willing to sign a Human Research Protection Office (HRPO) approved written informed consent document (or that of legally authorized representative, if applicable)
+Participants must be able to understand and be willing to sign a written informed consent document
+Patients must sign informed consent
+Patients must be able to understand and willing to sign a written informed consent document.
+Willing and able to give informed consent
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Understand and voluntarily sign an informed consent form
+Failure to sign informed consent
+Patients must be able to understand and willing to sign an informed consent
+Must be able to read, understand and sign informed consent
+Able to sign informed consent and to comply with the protocol
+Willing and able to comply with the protocol and sign informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Willing and able to give written informed consent
+Able to understand and willing to sign informed consent form (ICF)
+Able to comprehend and willing to sign an Informed Consent Form (ICF)
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Willing and able to give informed consent
+Willing and able to understand and sign informed consent form
+Able to give informed consent
+Able and willing to give valid written informed consent.
+Patient must be able to understand and willing to sign a written informed consent document
+Subjects unable to review and sign informed consent form
+Patients must sign an approved informed consent document
+Able to sign voluntary written informed consent
+Patients must be able to understand and sign informed consent
+Understand and voluntarily sign an informed consent form
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to understand and sign informed consent
+Patient is aware of her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Willing and able to sign informed consent
+Patient must be able to understand and willing to sign a written informed consent document
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Patients who are not able to sign inform consent
+Subjects or their guardians must be able to understand and be willing to sign the written informed consent form. A signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure.
+Subjects must be able to give written consent to the study
+Able to understand and willing to sign written informed consent document
+PRE-REGISTRATION INCLUSION CRITERIA: Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
+Must understand and voluntarily sign an informed consent form
+All patients must sign informed consent
+Each patients must be willing to participate as a research subject and must sign an informed consent form
+Patients must be able to understand and be willing to sign a written informed consent document
+Able to participate in the informed consent process
+Able to provide informed consent and be willing to sign an informed consent form
+Patient refuses to sign informed consent
+Understand and voluntarily sign an informed consent form
+Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
+able understand and give written informed consent and comply with the study protocol.
+Be willing and able to give written informed consent, and be able to comply with all study procedures
+Able to understand and to sign a written consent document
+Patients must sign a study-specific informed consent form
+Patient must be willing and able to sign the informed consent form
+Patients must be willing and able to sign the informed consent form, and to follow the study visit schedule and other protocol requirements.
+Willing and able to give written informed consent
+Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent
+Patients must sign a study-specific consent form
+Understand and voluntarily sign an informed consent form
+DONOR: Donors must be able to understand and sign informed consent
+Willing and able to give written informed consent
+Understand and voluntarily sign an informed consent form
+Patients must sign the informed consent form before registration
+Willing and able to give written informed consent
+Understand and voluntarily sign an informed consent form.
+Patient or patient’s legal representative, parent(s) or guardian able to sign informed consent
+Able to understand and sign the informed consent document
+Must understand and voluntarily sign an informed consent document.
+Able to understand and sign an informed consent (or have a legal representative who is able to do so)
+Patient must sign the informed consent document
+Patients must be able to understand and be willing to sign a written informed consent document
+Patient must understand and voluntarily sign an informed consent form
+Understand and voluntarily sign an informed consent form
+Must be able to understand and sign the informed consent document
+Patients must sign an informed consent
+Understand and voluntarily sign an informed consent form
+Understand and voluntarily sign an informed consent form
+Subject must understand and sign the study specific informed consent
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Written informed consent provided before any study-specific procedures are initiated. Subject must be able to understand and be willing to sign a written informed consent form.
+Patient refuses to sign informed consent
+Able to understand and sign the Informed Consent document
+Must sign an informed consent form.
+Be able to understand and sign informed consent
+Willing and able to sign informed consent
+Must understand and voluntarily sign an informed consent form.
+The patient or legal guardian must be able to comprehend the informed consent form and sign prior to patient enrollment
+The patient or legal guardian is able to give informed consent
+Patient or legal guardian must be able to give informed consent
+Patients must sign informed consent prior to study entry
+Patients must be able to give informed consent
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Patients must sign a study-specific informed consent form prior to treatment
+Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines
+Able to comprehend and willing to sign the written informed consent form
+Patients must sign written informed consent
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Able to give informed consent.
+Able to understand and sign informed consent
+Patient is willing to sign study specific informed consent
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Able to understand and sign the informed consent document
+Able to understand and sign the informed consent document
+Able to sign an informed consent
+Able to understand and sign the informed consent document
+Patient or patient’s legal representative, able to sign informed consent
+Able and willing to give valid written informed consent.
+Patients must be able to understand and willing to sign a written informed consent document
+All patients must be able to comprehend and sign informed consent
+TREATMENT: Patients must be willing to sign the standard informed consent
+Patients or their legal representative must be able to read, understand and sign an informed consent form (ICF)
+Able to understand and sign the informed consent document
+RECURRENT/ PROGRESSIVE DIPG (STRATUM 1): The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
+NON-PROGRESSED DIPG (STRATUM 2): The patient or parent/guardian is able to understand the consent and is willing to sign a written informed consent document according to institutional guidelines
+Able to understand and willing to sign the informed consent form
+Willing and able to give written informed consent
+Willing and able to sign the informed consent and to comply with the protocol for the duration of the study.
+Ability to understand and sign informed consent form (ICF) and comply with treatment protocol
+All subjects must be able to comprehend and sign a written informed consent document
+Understand and voluntarily sign an informed consent form
+Patient must be able to understand and be willing to sign a written informed consent document
+Able to understand and sign a consent form
+Patients must sign an informed consent form
+Patient able to understand and willing to sign and date the written voluntary informed consent form (ICF) at screening visit prior to any protocol-specific procedures
+Must sign an approved informed consent
+Able to give informed written consent
+Able to understand and willing to sign the informed consent form
+Be able to give informed consent
+Patient must be able to understand and willing to sign a written informed consent document
+Able to understand and sign the informed consent document
+Patient or a legally authorized representative of a patient must be able and willing to sign informed consent document that has been approved by an IRB
+Ability to understand and voluntarily sign an informed consent form
+Patients must be able to understand and be willing to sign a written informed consent document
+All patients must sign a written informed consent
+Must be able to read and understand informed consent
+Adults must be able to understand and sign the informed consent document
+Patient or legally authorized representative able to sign an informed consent form
+Patient or legally authorized representative able to sign informed consent
+Patients must be able to understand and voluntarily sign an informed consent form
+Willing and able to understand and voluntarily sign a written informed consent
+Able to understand and sign an informed consent (or have a legal representative who is able to do so)
+Able and willing to give written informed consent.
+All patients must sign an informed consent prior to enrollment
+Able to sign informed consent and to comply with the protocol
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Patients must be able to read, understand and sign informed consent
+Able to understand and sign the informed consent document
+Able to understand and sign the informed consent document
+Patients of their legal representatives must be able to understand and sign an informed consent form
+Able to give informed consent
+Be willing and able to give written informed consent, and be able to comply with all study procedures
+Donor must be able to understand and willing to sign an IRB approved written informed consent document. Recipient Inclusion Criteria
+Recipient must be able to understand and willing to sign an IRB approved written informed consent document.
+Able to understand and willing to sign an informed consent form (ICF) prior to initiation of any study-specific procedure and treatment
+Willing and able to give informed consent
+Patient must be able to understand and willing to sign a written informed consent document
+Understand and voluntarily sign informed consent form
+Subjects must be willing to give written informed consent and be able to adhere to dose and visit schedules.
+Refusal to sign informed consent
+Must sign an Informed Consent Form (ICF)
+Patient must be able to give informed consent
+Must understand and voluntarily sign informed consent form
+Able to sign informed consent and to comply with the protocol
+Patients must be capable and willing to sign informed consent
+Ability to understand and voluntarily sign an informed consent form
+Patients must be willing to sign an informed consent
+Able to understand and sign the Informed Consent Document
+Able to understand and sign the informed consent document
+Patients or guardian able to sign informed consent
+Patient is able to give and sign study specific informed consent
+Willing and able to give written informed consent
+Patients must be able to render informed consent and must consent to participate in the trial
+Must sign a written informed consent,
+Willing to consent to randomization and able to participate in the study
+Both parties are required to sign an informed consent
+Unwilling to sign an informed consent
+Each patient must be willing to participate as a research subject and must sign an informed consent form
+Able to give informed consent
+Patients must sign written informed consent
+Patients able to understand the nature of the study and who are willing to give written informed consent;
+The patient must be able to understand the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Subject is able to read, understand, and sign a written Informed Consent to participate in the study.
+Patients must sign a study-specific consent form
+Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Able to give consent
+All subjects must be able to comprehend and sign a written informed consent document
+Patient able to understand and the willingness to sign a written informed consent
+Able to give written informed consent
+Able to give informed consent
+Able to understand and willing to sign an IRB-approved written informed consent document
+Both patient and caregiver willing to give and sign informed consent
+PARTNER: Able to consent to the study
+Able to understand and willing to sign a written informed consent document
+Patients must have the ability to understand and read English, sign a written informed consent, and be willing to follow protocol requirements
+Potential participant/guardian is willing to sign informed consent
+Patient and/or parents/guardians as appropriate must sign an informed consent, be mentally responsible, able to understand and willing to sign a written informed consent
+Able and willing to give informed consent
+Able and willing to sign protocol consent form
+Individual is willing to sign written informed consent
+Patients must have the ability to understand and read English, sign a written informed consent, and be willing to follow protocol requirements.
+Able and willing to give informed consent
+Able to understand and sign the informed consent
+Able and willing to sign informed consent/assent
+Willing to sign consent
+Able to understand and willing to sign a written informed consent document
+Subjects who are able to understand and sign an informed consent document
+Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Able to give informed consent
+Able to give informed consent
+All subjects must be able to comprehend and sign a written informed consent document
+Subjects must be able to understand and be willing to sign the written informed consent form; a signed informed consent form must be appropriately obtained prior to the conduct of any trial-specific procedure
+Patients must sign an informed consent
+FAMILY CAREGIVER: Able and willing to consent
+SCREENING PHASE: The patient is aware of the nature of his/her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+INTERVENTION PHASE: The patient is aware of the nature of his/her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Able to give informed consent
+Are able to give consent
+Participants are able to give consent
+Participants are eligible if they are able to give consent
+Are eligible if they are able to give consent
+Patients and caregivers must both be able to give informed consent
+The patient must sign consent for study participation
+Participants must be able to understand and willing to sign a written informed consent document
+Participants must be able to understand and be willing to sign a written informed consent document
+Able to sign informed consent
+Inability to sign an informed consent form prior to registration on study
+Patients able to render informed consent and to follow protocol requirements
+Capacity to understand and sign the study informed consent form
+Subjects must sign informed consent
+Be able to understand the description of the study and give written informed consent
+Able to understand and sign the informed consent
+Able to give informed consent
+Able to understand and sign consent
+All patients must sign a written informed consent
+Willing to sign informed consent
+The patient is aware of the nature of her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent document
+Patients must be able to sign informed consent
+Willing and able to read, understand and sign an informed consent form (ICF)
+Subjects are able to give informed consent
+The patient understands the study requirements and is willing and able to sign an informed consent document
+Willing and able to understand and sign consent form
+Patients must sign a study-specific consent form
+Able to give informed consent
+Able to give informed consent
+Adult patients must be able to understand and sign a written informed consent. For minor patients, the parent/legal guardian or representative must be able to understand and sign a written informed consent. Assent, when appropriate, will be obtained according to institutional guidelines.
+Able to give informed consent
+Participants must be able to understand and willing to sign a written informed consent document
+Patients sign the informed consent
+Able to give informed consent
+Patient, parent/guardian able to give informed consent
+Understand and voluntarily sign an informed consent form
+Able to fully understand and participate in the informed consent process
+Patients who are able to understand and give consent to participating in the study
+Ability to comprehend and sign informed consent
+Ability to sign informed consent
+Able to give consent
+Patient is able to understand and give consent to participation in the study.
+Provision to sign and date the consent form
+Patient is able to sign a study specific informed consent form
+Willing and able to sign consent form.
+Sign informed consent
+Ability to sign an informed consent
+Subjects who refuse to give and/or sign the informed consent
+Able to understand and willing to consent or assent to the research proposed, along with consent of legal guardian(s) if applicable
+Able to consent for the study
+All subjects must be able to give informed consent
+Voluntarily agree to participate and sign an informed consent document
+Patients must be able to read, understand, and voluntarily sign an informed consent document
+Willing and able to give informed consent and adhere to visit/protocol schedules
+Patient must be able to understand and willing to sign a written informed consent document
+Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
+Patients who agree to sign an informed consent to undergo MBI
+Adults with a suspected or confirmed lymphoma diagnosis and:\r\n* Who will undergo clinically indicated procedure potentially allowing for excess or discarded clinical specimens\r\n* Who must be able to understand and sign an informed consent
+Patients must sign an informed consent form for study
+Patients/subjects able to give informed consent
+Patient is able to give informed consent for this study
+Subject is able to give informed consent for this study
+Able to give informed consent
+Patient is able and willing to give valid written informed consent
+Understands the trial and procedure and is willing and able to sign the informed consent form
+Refusal to sign the informed consent
+Patient understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+AIMS 1 AND 2: Participants must be able to understand and willing to sign a written informed consent document
+AIM 3: Participants must be able to understand and willing to sign a written informed consent document
+Able to give written informed consent to participate in the study
+Patient must be able and willing to give informed consent
+Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
+Able to give informed consent
+Patient or legally authorized representative must be able to understand and willing to sign a written informed consent document
+Subjects must be willing and able to understand and sign informed consent
+Ability to sign informed consent
+Willing and able to consent and participate in the study.
+Subject must be willing and able (in the opinion of the investigator) to understand the informed consent form
+Is able to agree to and sign informed consent and to comply with the protocol
+Able to give consent
+Subjects must be able to understand and willing to sign a written informed consent form
+Able to understand and willing to sign a written informed consent document
+Able to understand and willing to sign a written informed consent document
+Must understand and voluntarily sign an informed consent form after the contents have been fully explained to them
+Women who are not able to give consent
+The patient is aware of the nature of her diagnosis, understands the study regimen, its requirements, risks, and discomforts, and is able and willing to sign an informed consent form
+Patient must sign informed consent to participate in the study
+The patient does not sign the informed consent
+Patient (or legally authorized representative) must be able to understand and willing to sign a written informed consent document
+Patients must be able to understand and willing to sign an informed consent
+Patients must sign an informed consent document
+Must be able to understand and sign a written informed consent document
+Willing and able to give informed consent
+Patients must be able to understand and willing to sign an informed consent
+Able to understand and sign an informed consent document (or has a legal representative who is able to do so)
+Surgeon: Able to understand and willing to sign an IRB-approved written informed consent document
+Nurse: Able to understand and willing to sign an IRB-approved written informed consent document
+Able to understand and willing to sign an IRB-approved written informed consent document
+Patients must be able to understand and be willing to sign a written informed consent document to participate
+The patient must be able to give informed consent
+Patients must sign an informed consent
+Patients who are able to understand the investigational nature of this study and agree to sign a written informed consent document
+Patients willing to give informed consent
+Sign an approved informed consent form for this study.