--- a
+++ b/clusters/3009knumclusters/clust_29.txt
@@ -0,0 +1,722 @@
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed, dated informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Voluntary signed informed consent (IC)
+Signed informed consent
+Patients must have given signed, informed consent prior to registration on study
+Signed and dated informed consent
+Subject has the ability to understand and provide signed informed consent
+Procurement: Informed consent explained to, understood by and signed by patient. Patient given copy of informed consent
+Informed consent explained to, understood by and signed by patient. Patient given copy of informed consent
+Signed, written IRB-approved informed consent
+Signed written informed consent
+Written and voluntary informed consent understood, signed and dated.
+Ability to provide signed Informed Consent Form
+Signed written informed consent
+Be 18 years of age at the time the informed consent form is signed
+Signed informed consent prior to any procedures
+Signed informed consent
+Provide signed, written informed consent.
+Patients must have signed an approved informed consent
+Ability to understand and the willingness to sign a written informed consent document; NOTE: consent documents can be signed up to 30 days prior to registration; if > 30 days has elapsed since patient signed the consent document, s/he must re-consent (new signature) before proceeding to register onto study
+Signed and dated written informed consent obtained prior to any study-specific evaluation.
+Dated and signed IEC/IRB-approved informed consent.
+Signed written informed consent
+The subject is capable of understanding and complying with the protocol and has signed the informed consent document
+Signed informed consent obtained prior to any screening procedures
+The patient must be able to comprehend and have signed the informed consent
+Patients must have signed an approved informed consent and authorization permitting the release of personal health information
+Signed informed consent
+All subjects must have given signed, informed consent prior to registration on study
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed informed consent MUST be obtained from patient or parent/legal guardian (if patient is less than 18 years of age). Consent must be signed prior to any study procedures and study entry
+Signed informed consent/assent
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Evidence of a signed informed written consent
+The subject is capable of understanding and complying with the protocol and has signed the informed consent document
+The subject is capable of understanding and complying with the protocol and has signed the informed consent document
+Patient has signed informed consent
+Signed informed consent.
+Participant has signed informed consent form (ICF) before any trial related activities and according to local guidelines.
+Evidence of a signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the study
+PROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient; patient given copy of informed consent
+Informed consent explained to, understood by and signed by patient; patient given copy of informed consent
+INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+INCLUSION - TREATMENT: Informed consent explained to, understood by, and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed and dated written informed consent
+The subject is capable of understanding and complying with the protocol and has signed the informed consent document
+Signed informed consent according to institutional guidelines must be obtained
+Be 18 years old at the time the informed consent form is signed
+The participant is capable of understanding and complying with the protocol and has signed the informed consent document
+Signed informed consent for the study protocol
+INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given a copy of informed consent
+INCLUSION - INFUSION: Informed consent explained to, understood and signed by patient/guardian; patient/guardian given a copy of informed consent
+Subject has signed and dated informed consent
+PROCUREMENT INCLUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+TREATMENT INCLUSION: Informed consent explained to, understood by and signed by patient or guardian; patient or guardian given a copy of the informed consent form
+Has provided signed written informed consent
+Signed informed consent
+• Subject signed inform consent
+Written and voluntary informed consent understood, signed and dated.
+Signed written informed consent obtained prior to study procedures
+In the opinion of the Investigator, the patient is capable of understanding and complying with the protocol and has signed the informed consent document.
+Voluntarily signed and dated written informed consent prior to any specific-study procedure.
+Signed informed consent
+Provision of signed written informed consent
+Signed donor and patient/guardian informed consent;
+PHASE I: Signed informed consent
+PHASE IB: Signed informed consent
+Show evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial.
+Subjects must be able to understand and be willing to sign the written informed consent form; ideally, a signed informed consent form will be appropriately obtained prior to the conduct of any trial-specific procedure; however, if patients have had standard of care assessments performed within the screening period, but before the consent was signed, these will be admissible
+ELIGIBILITY CRITERIA AT TIME OF TREATMENT: Informed consent (and assent as applicable) signed by patient/guardian
+Signed written informed consent.
+PROCUREMENT INCLUSION CRITERIA: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed informed consent form
+Failure to provide signed informed consent
+Patient or authorized proxy needs to have signed the informed consent form
+Able to provide signed informed consent (or consent provided by legal guardian for pediatric patients, as applicable)
+Understand study design, risks, and benefits and have signed informed consent
+INCLUSION - PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+INCLUSION - TREATMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
+Patient has signed and dated informed consent
+Patients must consent to be in the study and must have signed and dated an approved consent form, which conforms to federal and institutional guidelines
+The patient must be competent and have signed informed consent
+Ability to sign an informed consent; can be signed by family member or health care proxy; informed consent must be done prior to registration on study
+All patients must have given signed, informed consent prior to registration on study
+Signed and dated written informed consent.
+Signed written informed consent.
+Signed and dated written informed consent.
+Signed informed consent
+Signed, informed consent
+Signed Informed consent form
+Signed and dated written informed consent obtained from patient or legal representative.
+Eligible and consent signed for imaging with AMT PET under protocol 2011-­053
+Evidence of a personally signed informed consent document.
+Written informed consent and/or signed assent from patient, parent or guardian.
+The patient has not signed a study-specific informed consent for this study.
+STUDY ENTRY: Signed Informed Consent Form (ICF).
+Signed and dated informed consent
+Provide signed written informed consent
+Capable of understanding and complying with the protocol requirements and has signed the informed consent document.
+Patients must have signed an informed consent document stating that they understand the investigational nature of the proposed treatment
+Signed written informed consent
+Signed informed consent
+Provision of signed and dated informed consent form (ICF).
+The participant is capable of understanding and complying with the protocol and has signed the informed consent document
+Signed Informed Consent Form.
+Signed informed consent according to institutional guidelines must be obtained prior to registration
+Evidence of a personally signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the study
+Signed informed consent document and assent when appropriate
+Signed written informed consent obtained prior to study procedures
+Signed informed consent.
+Signed and dated written informed consent
+Subjects must be able and willingly give signed informed consent
+Signed informed consent
+Ability to understand and provide signed informed consent
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed informed consent form (ICF) and comply with the requirements of the study protocol
+Have signed informed consent to participate in the study
+Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Signed informed consent
+signed written informed consent obtained prior to study procedures
+Signed informed consent indicating awareness of the investigational nature of this program
+Provision of signed informed consent.
+Signed informed consent form (ICF)
+Signed informed consent
+Participants signed informed consent
+Signed informed consent
+Have signed written informed consent
+Signed informed consent.
+Subject has signed and dated informed consent
+Provision of signed written informed consent.
+Signed informed consent
+Patient must have the ability to understand the requirements of the study and signed informed consent. A signed informed consent by the patient or his legally authorized representative is required\r\nprior to their enrollment on the protocol
+Capable of understanding and complying with the protocol and has signed the informed consent document
+Signed study-specific informed consent
+Signed, informed consent
+Signed informed consent form (ICF)
+Signed informed consent obtained prior to any screening procedures
+Signed informed consent;
+Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Patient has the ability to understand and provide signed informed consent
+Signed informed consent;
+Provide signed Informed Consent
+Signed consent to long-term follow-up protocol PA17-0483.
+Signed informed consent form (ICF)
+Signed informed consent form (ICF)
+The patient is capable of understanding and complying with the protocol and has signed the informed consent document. A signed informed consent form must be obtained before any study-specific procedures are performed.
+Signed and dated written informed consent
+Signed written informed consent
+>=18 years of age and provided signed written informed consent
+Signed informed consent
+Signed and dated written informed consent prior to admission to the study
+Signed informed consent
+Informed consent signed by the subject
+Subject has been informed of the study procedures and the treatment and has signed an informed consent form
+Signed written informed consent
+Signed informed consent
+Signed informed consent form in accordance with institutional and federal law policies
+Capability to understand and comply with the protocol requirements as and signed informed consent documents
+Signed, written informed consent
+Signed written informed consent
+Subjects must have signed written, informed consent
+Capable of giving signed informed consent
+Signed informed consent document(s)
+Signed informed consent form in accordance with institutional policies prior to the initiation of high-dose therapy
+Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Provide signed written informed consent
+Signed informed consent on protocol LAB02-188
+Have signed an informed consent document
+Signed informed consent by patient and/or parents or legal guardian
+Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study
+Signed, informed consent
+Signed informed consent according to institutional guidelines prior to registration.
+Informed consent obtained and signed
+Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment.
+Signed informed consent indicating awareness of the investigational nature of this program
+Signed, written informed consent
+Signed study-specific consent form
+Signed informed consent
+Signed informed consent form must be obtained prior to any research procedure
+Informed consent reviewed and signed
+Signed written informed consent
+Signed written informed consent must be obtained prior to any study procedures.
+Subjects must have signed written, informed consent
+Signed written informed consent
+Signed informed consent obtained prior to any screening procedures
+Signed consent
+Signed informed consent
+Have signed the current approved informed consent form
+Signed informed consent indicating awareness of the investigational nature of this program
+Written informed consent from patient and/or signed assent from patient, parent or guardian
+Signed written informed consent form
+Ability to understand and provide signed informed consent
+Signed informed consent obtained prior to any screening procedures
+Subject understood and signed the study specific informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed, written, informed consent
+AT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of informed consent
+AT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by research subjects/guardian; subject/guardian given copy of informed consent
+Patients who have signed informed consent and authorization permitting release of personal health information
+Signed informed consent
+PROCUREMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copy
+TREATMENT: Informed consent explained to and signed by patient/guardian able to give informed consent and patient given a copy
+Signed and dated informed consent form indicating that the patient has been informed of all pertinent aspects of the trial prior to enrollment
+Signed informed consent obtained prior to any screening procedures
+Patient has signed informed consent and is willing to comply with the protocol
+Capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Patient has the ability to understand and provide signed informed consent
+Informed consent form signed by the subject
+A signed and dated written informed consent form is obtained from the subject
+Informed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.
+Ability to understand and provide signed informed consent
+Written informed consent and/or signed assent line from patient, parent or guardian
+Signed informed consent
+Signed informed consent
+The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
+COHORT II: The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Provide signed written informed consent
+Signed informed consent
+Signed and witnessed informed consent and signed authorization for the release of their protected health information
+Patient must have the ability to understand the requirements of the study and signed informed consent a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
+Signed informed consent
+Written informed consent and/or signed assent line from patient, parent or guardian
+Signed informed consent indicating awareness of the scheduling and side effects, as well as testing requirements, of this program
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed informed consent form must be obtained prior to any study procedure
+Signed informed consent obtained prior to any screening procedures
+Signed informed consent
+Signed informed consent
+All patients must have given signed, informed consent prior to registration on study
+Patients must have signed an approved informed consent
+Signed informed consent document(s)
+Signed Informed Consent Form
+Ability to understand and provide signed informed consent that fulfills Institutional Review Board’s guidelines
+Provide signed written informed consent
+Signed informed consent prior to initiation of any study-specific procedure or treatment
+Signed informed consent
+Signed and dated written informed consent
+Patient (if ? 18 years old), or patient's legal representative(s) must have signed informed consent
+Signed informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Patient has signed the informed consent document agreeing to the use of the study drug, domperidone
+Signed informed consent
+Signed and dated written informed consent
+Informed consent obtained and signed
+Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
+Signed written informed consent
+Signed study-specific informed consent prior to study entry
+Patients must have signed an approved informed consent
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Informed consent explained to, understood and signed by patient/guardian; patient/guardian given copy of informed consent
+Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
+Signed informed consent
+Signed informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Provided signed informed consent.
+Signed written pre-registration informed consent document
+Signed written informed consent\r\n* The signed informed consent\r\n* The benefits/risks of the induction chemotherapy regimen will be reviewed, and a second consent may be necessary if the regimen will be administered according to a separate protocol
+Signed informed consent according to institutional guidelines must be obtained
+Signed informed consent
+Signed informed consent by the patient or legally authorized representative
+Written informed consent and/or signed assent line from patient, parent or guardian
+The patient must consent to be in the study and must have signed an approved consent form conforming with federal and institutional guidelines
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Informed Consent: Signed by the subject prior to screening.
+Consent signed
+PART II: The Part 2 consent must be signed
+Signed informed consent indicating awareness of the investigational nature of this program
+Signed study-specific informed consent form prior to study entry
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed informed consent
+Signed study-specific consent form prior to registration
+Signed study-specific informed consent prior to study entry
+Signed informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Signed informed consent indicating awareness of the investigational nature of this program
+Provide signed informed consent
+Signed informed consent before initiation of any study procedures.
+Signed informed consent
+Signed and dated informed consent of the patient, available before the start of any specific trial procedure.
+Signed informed consent form
+Signed informed consent form
+Signed informed consent form
+Signed informed consent
+Patients must have voluntarily signed an informed consent in accordance with institutional policies.
+All patients must have given a signed, informed consent prior to enrollment on study
+Signed informed consent.
+Signed written informed consent per institutional and federal regulatory requirements
+Patients who have signed informed consent for this long term extension program.
+Signed informed consent
+Have signed a written informed consent
+Subjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
+Signed and dated informed consent document.
+Signed informed consent
+Capable of giving signed informed consent.
+Signed written informed consent
+Signed consent to long-term follow- up protocol PA17- 0483
+Signed informed consent form (ICF).
+Signed informed consent on protocol LAB02-188.
+Signed and dated informed consent document indicating that the patient has been informed of all pertinent aspects of the trial prior to randomization
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+ENROLLMENT: Signed informed consent and if applicable pediatric assent.
+Signed informed consent form.
+Signed informed consent for protocol PA13-0291
+Patient must have the ability to understand the requirements of the study and signed informed consent; a signed informed consent by the patient or his legally authorized representative is required prior to their enrollment on the protocol
+Informed consent document signed and dated by patient
+Patients must provide a signed informed consent form before any trial relates activities are carried out.
+Signed written informed consent.
+Provide signed informed consent
+The patient must signed an informed consent form (ICF).
+Signed & dated informed consent prior to Screening evaluations
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed informed consent.
+Subjects must provide a signed informed consent before any screening procedures
+Signed informed consent form (ICF)
+Signed informed consent for the focal laser ablation (FLA) treatment through the 12 month follow up visit
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting the release of personal health information
+Able to provide signed, informed consent
+Signed informed consent according to institutional guidelines must be obtained
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Ability to understand and sign the informed consent; patient must have signed informed consent prior to registration on study
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed and informed consent to participant in this study
+Signed informed consent to participate in this study
+Patients must have signed an approved informed consent
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment
+Signed informed consent
+Signed informed consent by the patient or the patient's parent or guardian for patients who are minors
+Signed informed consent
+Patients must have signed an approved informed consent and authorization permitting the release of personal health information
+Capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed and dated written informed consent to participate in this clinical trial must be obtained prior to any study procedure
+Patient is willing to participate in the study and has signed the study informed consent
+Signed, written IRB-approved informed consent.
+Signed informed consent
+Patients must have signed an approved informed consent
+Voluntary signed informed consent form (ICF).
+Signed study-specific consent form prior to registration
+Signed study-specific informed consent
+Signed written informed consent
+Signed informed consent
+A signed informed consent form or minor assent form
+Provide signed and dated informed consent indicating that the patient has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.
+Signed written informed consent
+Signed informed consent prior to any study-related evaluation
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+A signed informed consent form or minor assent form
+Patients must have been off of chemotherapy for at least 4 weeks prior to day 1 of cycle 1; informed consent can be signed at any time prior to the start of therapy
+Signed informed consent form
+Signed informed consent
+Signed study specific informed consent form;
+Signed informed consent prior to any protocol-specific procedures
+Signed informed consent
+Patient has provided a signed study informed consent form prior to performance of any study related procedure
+Signed written informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information.
+Signed study-specific consent form prior to registration
+Subjects >=18 years of age and provided signed written informed consent.
+Signed informed consent
+Signed and dated informed consent.
+Signed informed consent document
+Informed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copy
+Informed consent explained to and signed by patient or parent/guardian able to give informed consent and given a copy
+Signed informed consent form
+Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Participant is able to provide signed informed consent
+Capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Be 18 years old at the time the informed consent is signed
+Signed, written informed consent by subject or legal representative prior to any trial-specific screening procedure
+Signed informed consent obtained prior to any screening procedures
+Signed informed consent
+All patients must have given signed, informed consent prior to registration on study
+Signed, written informed consent
+All subjects must have given signed, informed consent prior to registration on study
+Signed informed consent in accordance with federal, local, and institutional guidelines
+Patients must have signed an IRB-approved informed consent and authorization permitting release of personal health information.
+Signed, written, informed consent
+Capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed written informed consent.
+Patients must have signed an approved informed consent and authorization permitting the release of personal health information
+Signed informed consent
+Signed informed consent
+Signed written informed consent
+The patient has provided signed informed consent
+The patient has signed the study-specific informed consent form
+Signed written informed consent for this protocol
+Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Must provide a signed and dated informed consent indicating that the participants has been informed of all pertinent aspects of the study, including the potential risks, and is willingly participating.
+Provision of signed and dated, written informed consent
+AT THE TIME OF PROCUREMENT: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+AT THE TIME OF INFUSION: Informed consent explained to, understood by and signed by patient/guardian; patient/guardian given copy of informed consent
+Signed informed consent form
+Patient has the ability and willingness to provide informed consent and has signed the informed consent document
+Signed written informed consent
+Signed written informed consent
+Informed consent reviewed and signed
+Patient has signed a written informed consent.
+Provide signed informed consent
+Signed, written informed consent.
+Signed informed consent form (ICF)
+Signed and dated informed consent.
+Signed informed consent
+Has provided a signed informed consent
+Signed written informed consent
+Signed informed consent
+All patients must have given signed, informed consent prior to registration on study
+Signed Informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Informed consent and authorization for the release of health information signed by the patient
+Signed written informed consent granted
+All patients must have given signed, informed consent prior to registration on study
+Signed written informed consent
+STEP 2 ENROLLMENT AND RANDOMIZATION: the patient has signed informed consent
+Signed, written informed consent
+Signed informed consent
+Willingness and ability to give signed written informed consent
+Signed informed consent indicating awareness of the investigational nature of this program
+Patients must have signed an approved informed consent
+Signed a protocol-specific informed consent
+Signed informed consent
+Signed study-specific informed consent
+Signed informed consent
+Signed informed consent from patients and/or their parents or legal guardians
+The participant is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Patients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.
+Signed informed consent
+Has provided signed informed consent for this study.
+An approved informed consent must be signed by the patient
+Signed informed consent from patients and/or their parents or legal guardians
+An approved informed consent and authorization permitting release of personal health information must be signed by patient or guardian
+Signed informed consent document
+All subjects must have given signed, informed consent prior to registration on study
+Signed informed consent by patient and/or parents or legal guardian
+Voluntarily signed informed consent.
+Signed Informed Consent
+Has provided signed informed consent for this study.
+Understand and voluntarily signed informed consent
+An approved Informed Consent and authorization permitting release of personal health information must be signed by the patient or guardian
+Patients must give written informed consent; a copy of the signed informed consent form will be retained in the patient’s chart
+Signed written informed consent;
+Signed and dated IRB/Approved Informed Consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed informed consent
+Has provided signed written informed consent for this study
+Signed study-specific informed consent
+A signed study specific consent form is required
+Signed written informed consent to Study ARQ 197-299
+Signed informed consent form (ICF)
+Signed written informed consent.
+Signed written informed consent.
+Patients must have signed an approved informed consent and authorization permitting release of personal information
+Signed study-specific informed consent prior to registration
+Signed, written informed consent
+Signed informed consent document and assent when appropriate
+The patient must consent to be in the study and must have signed an approved consent form conforming to institutional guidelines
+signed written informed consent
+Signed informed consent according to institutional guidelines must be obtained
+Patients who have signed an approved Informed Consent
+Signed informed consent
+Signed informed consent
+Have signed an approved informed consent form for the study.
+Able and willing to give voluntary, written and signed, informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Provided signed written informed consent
+Signed Informed Consent Form (ICF)
+Provision of a signed informed consent
+Signed informed consent
+Provision of a signed informed consent
+Signed informed consent
+Signed written informed consent
+Signed informed consent prior to the start of systemic therapy; in the event of enrollment of a minor patient, an attempt to obtain assent from the patient must be documented, and parental consent must be signed
+Signed and dated written informed consent prior to admission to the study
+Signed IRB approved Informed Consent Form (ICF).
+Signed, approved Informed Consent.
+Able to understand and have signed an approved consent form that conforms to federal and institutional guidelines
+Signed informed consent
+Provide signed written informed consent
+Signed informed consent
+Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
+Subject has signed and dated informed consent
+Provided signed written informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Procurement consent signed and faxed to Research Coordinator
+Signed informed consent
+Signed informed consent
+Patient must have signed informed consent prior to registration on this study
+Signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Subjects ? 18 years of age who have signed informed consent
+Signed informed consent, which indicates the investigational nature of this study, is required
+TREATMENT: Patients must have signed the screening consent
+Signed written informed consent
+Patients must have signed an approved informed consent
+Written and signed informed consent must be obtained
+Signed informed consent form (ICF)
+Patients must have signed an approved informed consent.
+Signed Informed Consent Form
+Signed Informed Consent Form
+Voluntary signed, written IRB-approved informed consent.
+PRE-REGISTRATION INCLUSION CRITERIA: Signed and dated informed consent document for study participation
+Evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial
+Informed consent explained to, understood by and signed by patient/guardian. Patient/guardian given copy of informed consent.
+Signed Informed Consent Form
+Signed Informed Consent Form
+Voluntarily signed and dated written informed consent
+Voluntarily signed and dated written informed consent
+Signed the informed consent form (ICF)
+Evidence of a personally signed and dated written informed consent to participate in the clinical study
+Signed informed consent
+Patients must have a signed informed consent form prior to enrollment on study
+Signed written informed consent.
+Subjects, or subject's legal representative, who have provided signed informed consent, and assent when applicable, prior to participation.
+Unable to give signed informed consent
+Signed informed Consent
+Signed Informed Consent Form
+Signed informed consent from patient
+Informed consent obtained and signed
+A signed informed consent document (ICD)
+Patient (or legal representative) is able to understand and provide signed informed consent
+Signed informed consent
+Have signed written informed consent
+Signed and dated informed consent indicating that the subject (or legally acceptable representative if applicable by local laws) has been informed of all the pertinent aspects of the trial prior to enrollment
+Signed, written informed consent.
+Signed Informed Consent Form
+Signed written informed consent.
+Signed written informed consent
+Signed informed consent document
+Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
+Ability to provide written informed consent. Evidence of a personally signed informed consent.
+Signed Informed Consent.
+Signed written informed consent
+Signed Informed Consent Form
+Signed written informed consent
+Signed Informed Consent Form
+Written informed consent and/or signed assent line from patient, parent or guardian
+Signed informed consent
+Signed informed consent
+Signed informed consent form (ICF)
+Signed written informed consent
+Signed study-specific informed consent form
+Provide signed written informed consent
+Signed informed consent.
+Signed written informed consent
+Signed written informed consent provided
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed informed consent
+Signed and dated informed consent document indicating that the patient has been informed of all the pertinent aspects of the trial prior to enrollment
+Signed Written Informed Consent
+The signed informed consent form
+Voluntarily signed and dated written informed consent
+Signed informed consent
+Signed written informed consent
+All patients must have given signed, informed consent prior to registration on study
+Signed informed consent
+An approved informed consent and authorization permitting release of personal health information must be signed by the patient or guardian
+Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
+The subject has the capability of understanding the informed consent document and has signed the informed consent document
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Informed consent explained to and signed by parent/legal guardian or patient if the patient is >= 18 years
+Patient or legal guardian has signed informed consent.
+Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines
+Parents or legal guardian signed-written informed consent
+Patient and/or legal guardian able to provide signed informed consent
+Signed informed consent
+Signed and dated written informed consent
+Signed and dated informed consent document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
+Patients must have signed an approved informed consent and authorization form permitting the release of personal health information
+Signed written informed consent
+A personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
+Signed informed consent
+Written informed consent (IC) for trial participation must be signed and dated by the patient and the investigator prior to enrollment
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Written informed consent signed prior to entry into the study
+Signed ICF
+Signed and dated Informed Consent Form (by the patient or a legally acceptable representative as per the local regulations).
+Signed informed consent form
+Capable of giving signed, written informed consent
+Voluntary, signed informed consent
+All patients will have given signed, informed consent prior to registration
+(Patient participation) Signed written informed consent form
+Patient must provide signed informed consent.
+Provide signed and dated informed consent form
+Signed informed consent to the study
+Signed informed consent form
+Have read and signed study informed consent document (ICF)
+Signed informed consent
+All participants must have given signed, informed consent prior to registration in study
+Signed written informed consent
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Understands study design, risks, and benefits and have signed informed consent
+Signed informed consent
+Has signed consent within 6 months of diagnosis date
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Written informed consent form signed and dated by the subject
+Patient aged 12-17 years: has signed informed assent and their parent/legal guardian has signed informed consent for study participation
+Patient aged 18-25 years: has signed informed consent for study participation
+Able to understand and comply with the protocol requirements and has signed the informed consent document.
+Signed, written informed consent
+Signed informed consent on protocol LAB02-188
+Signed informed consent
+Signed informed consent`
+Signed informed consent
+Signed informed consent form from patient
+Signed informed consent
+Written informed consent and/or signed assent line from patient, parent or guardian
+Signed and dated informed consent
+Signed a study-specific informed consent prior to study entry
+Signed informed consent
+Signed informed consent
+Signed written informed consent prior to inclusion in the study.
+Patients must have signed an approved informed consent and authorization permitting release of personal health information
+Signed informed consent.
+Signed informed consent
+Signed written informed consent by parent(s)/legal guardians of the pediatric patient in compliance with the local laws and regulations. In addition signed children's assent form according to local requirements.
+Signed informed consent
+Signed informed consent
+Informed consent explained to, understood by and signed by subject/guardian; subject/guardian given copy of informed consent
+All patients must have given signed, informed consent prior to registration on study
+Signed informed consent
+Signed the 2 year extension study informed consent
+Signed informed consent
+An approved informed consent and authorization permitting release of personal health information must be signed by the patient or guardian
+Participants must have a signed written informed consent
+Signed and dated written IRB approved informed consent;
+Signed informed consent
+Evidence of a personally signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial
+Signed informed consent obtained prior to any screening procedures
+Provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
+Signed informed consent
+Signed informed consent
+Signed informed consent
+Signed informed consent obtained prior to any screening procedure
+Signed study-specific informed consent prior to registration
+Signed document of informed consent completed by the parent or legal guardian
+Signed informed consent
+All subjects must have given signed, informed consent prior to study registration
+Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained.
+For patients highly suspected to have aGVHD and requiring systemic therapy, informed consent should be signed after biopsy taken to support clinical diagnosis.
+For patients at high risk for developing aGVHD, informed consent should be signed prior to transplant.
+Provide signed and dated informed consent form
+Ability to provide signed informed consent and willingness to comply with protocol requirements
+Informed consent must be given and signed
+Willingness to signed informed consent
+Signed informed consent
+Signed, specific informed consent prior to study entry
+Signed, informed consent
+Signed informed consent
+Informed consent or assent signed by study subject or parent/guardian according to institutional guidelines
+Signed informed consent indicating awareness of the investigational nature of this study
+Signed written informed consent
+Patients must have signed informed consent
+Signed informed consent form
+Provide signed and dated informed consent form.
+Subjects must have signed an approved consent form
+Have signed informed consent to participate in the study
+Signed informed consent
+The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document
+Signed written informed consent and willingness to comply with protocol requirements
+Signed, specific informed consent prior to study entry
+Signed, written informed consent
+Patient has signed the informed consent (ICF) and is able to comply with protocol requirements
+Signed informed consent
+Patients with signed informed consent
+Signed informed consent
+Have signed Informed Consent to participate in the study
+Signed consent
+Signed consent
+Patients who have signed an approved informed consent form
+Have signed informed consent to participate in the study
+Signed informed consent of the patient
+Patients must have signed an informed consent
+Must understand and voluntarily have signed an Informed Consent after its contents have been fully explained
+Participants must be willing to participate and provide signed informed consent
+give signed informed consent prior to the initiation of therapy
+Signed informed consent for patient’s participating in the paper based survey
+Received and signed an informed consent form.
+Voluntarily signed and dated written informed consent prior to any specific study procedure.
+Signed informed consent form
+Signed Written Informed Consent
+The patient is capable of understanding and complying with the protocol and has signed the informed consent document.
+Signed informed consent form.
+Subjects must have received and signed an informed consent form.
+Voluntarily signed and dated informed consent
+Patient has the ability to understand and provide signed informed consent.
+Signed informed consent.
+Written informed consent will be signed by the patients before the MRI examination
+Subjects must have received and signed an informed consent form.
+Signed Informed Consent Form
+Written Informed Consent not obtained, signed and dated
+Signed written informed consent
+Before the patient is enrolled, the consent form, including any addenda, must be signed and dated by the patient and the person who explains the study to that patient
+Signed informed consent prior to any protocol-specific procedures