Documented informed consent
Patients must give informed consent prior to initiation of therapy
Informed consent/assent
Execute an informed consent.
Informed consent must be obtained from all patients prior to beginning therapy, including consent for mandatory tissue submission for ERCC1 staining (and p16 staining if not locally conducted); patients should have the ability to understand and the willingness to sign a written informed consent document
Have the capacity to give informed consent
Give informed consent
Refuses to give informed consent
Informed consent for participation
Have the capacity to give informed consent
Documented informed consent of the participant
Informed consent
Informed consent
Patients must give informed consent
Informed consent
Must have the capacity to give informed consent
Informed consent must be obtained
Informed Consent
Patients must give informed consent
Informed consent
Patients must give informed consent
Informed consent
Before any study procedures are performed, subjects will have the details of the study described to them, and they will be given a written informed consent document to read; then, if subjects consent to participate in the study, they will indicate that consent by signing and dating the informed consent document in the presence of study personnel
Patients must be informed of the investigative nature of the treatment, must give appropriate informed consent to protocol procedures and must sign an Informed Consent documentation form
Understand and give informed consent
Informed consent
Documented informed consent
Understand and give informed consent
Give informed consent
Refuses to give informed consent
Informed consent
Patient's Informed Consent. -
Before any study procedures are performed, subjects (or their legally acceptable representatives) will have the details of the study described to them, and they will be given a written informed consent document to read; then, if subjects consent to participate in the study, they will indicate that consent by signing and dating the informed consent document in the presence of study personnel
Informed consent
Patients must give informed consent
Informed consent
Parental informed consent
PHASE I: For patients < 18 years, parents must give informed consent and patient must give assent; patients >= 18 must give informed consent
PHASE II: For patients < 18 years, parents must give informed consent and patient must give assent; patients >= 18 must give informed consent
Informed consent
Subjects who cannot give an informed consent
Patient must give informed consent for this new study
Consent to the study; and
Refusal of informed consent
Patients must give informed consent
Cannot give informed consent.
Willingness to give informed consent
DONOR: Willingness to give informed consent
Informed consent
Documented informed consent of the participant
Women who cannot give an informed consent in English
Willingness to give informed consent
DONOR: Willingness to give informed consent
Subjects who cannot give an informed consent
Cannot consent for himself or herself
Patients cannot give informed consent.
Patients who cannot consent for themselves
Informed consent
Informed consent
Women who cannot consent for themselves
Patients who cannot consent for themselves
Patients who cannot give informed consent
Informed consent was obtained.
Patients must have capacity to consent
Patients willing to give informed consent