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+++ b/clusters/9knumclustersv2/clust_1115.txt
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+Patients must be able to understand and agree to sign an institutional review board (IRB)-approved informed consent form
+Is willing to voluntarily sign and date an informed consent form that is approved by an institutional review board before the conduct of any study procedure
+All subjects must have the ability to understand and the willingness to sign a written informed consent; signed informed consent form approved by the Institutional Review Board (IRB) is required; the patient, family member, and transplant staff physician (physician, nurse, and social worker) meet at least once prior to starting the transplant procedure; during this meeting, all pertinent information with respect to risks and benefits to the donor and recipient will be presented; alternative treatment modalities will be discussed
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigators Institutional Review Board (IRB)/Ethics Committee
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigators Institutional Review Board (IRB)/Ethics Committee
+All subjects must have the ability to understand and the willingness to sign a written informed consent that has been approved by the City of Hope Institutional Review Board (COH IRB); the patient, a family member and transplant staff physician (physician, nurse, social worker) will meet at least once prior to the subject signing consent; during this meeting all pertinent information with respect to risks and benefits to donor and recipient will be presented; alternative treatment modalities will be discussed; the risks are explained in detail in the enclosed consent form
+Ability to understand the purposes and risks of the study and has signed a written consent form approved by the investigators Institutional Review Board (IRB)/ethics committee
+Patient or durable power of attorney (DPA) for healthcare must be able to understand and voluntarily sign an Institutional Review Board (IRB) -approved informed consent form
+Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's IRB/Ethics Committee
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigators Institutional Review Board (IRB)/Ethics Committee
+Relapsed/refractory MCL: Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
+Patients must be able to understand and agree to sign an Institutional Review Board (IRB)-approved informed consent form
+Understanding and voluntarily signing an Institutional Review Board (IRB)-approved informed consent form
+Understand and sign, written Institutional Review Board (IRB)-approved informed consent form, and be willing to comply with all study procedures
+Patients must be able to understand and agree to sign an Institutional Review Board (IRB)-approved informed consent form
+FOR TISSUE COLLECTION TO ESTABLISH PDX (PART ): Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form.
+DONOR: The donor or legal guardian greater than  years of age, capable of signing an Institutional Review Board (IRB)-approved consent form
+Understanding and voluntary signing an institutional review board (IRB)-approved informed consent form
+Patients must exercise informed voluntary consent and sign a consent form approved by the University of Minnesota Institutional Review Board (IRB): Human Subjects Committee
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's Institutional Review Board (IRB)/Ethics Committee
+Understand and voluntarily sign an institutional review board (IRB)-approved informed consent form
+Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
+Patients must agree to randomization as documented by signing the Institutional Review Board (IRB) approved consent form
+Understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
+Understand and voluntarily sign an Institutional Review Board (IRB) approved informed consent form
+Understanding and voluntary signing an Institutional Review Board (IRB)-approved informed consent form
+Ability to read, understand, and sign a written informed consent approved by each Institutional Review Board (IRB); alternatively, patients with legal guardians who can read, understand, and sign written informed consent may also enroll
+Competent to sign and date an Institutional Review Board approved informed consent form
+Patient or durable power of attorney (DPA) for healthcare must be able to understand and voluntarily sign an Institutional Review Board (IRB)-approved informed consent form
+Able to understand and sign an Institutional Review Board (IRB)-approved informed consent form
+All subjects must have the ability to understand and the willingness to sign a written informed consent that has been approved by the City of Hope (COH) Institutional Review Board (IRB); the patient, a family member and transplant staff physician (physician, nurse, and social worker) will meet at least once prior to the subject signing consent; during this meeting all pertinent information with respect to risks and benefits to donor and recipient will be presented; alternative treatment modalities will be discussed; the risks are explained in detail in the enclosed consent form
+Ability to understand the purposes and risks of the study and has signed a written informed consent form approved by the investigator's Institutional Review Board (IRB)/Ethics Committee