Search Results 1361-1370 of 21179 for Informed consent
Unwilling or unable to obtain informed consent from the participant or substitute decision maker. Revascularization of coronary artery disease performed in ...
Participant is willing to give written informed consent; Age ≥ 21 years. Exclusion Criteria: LVEF < 35%; History of unprotected left main stenosis >50% on ...
Male or female subjects 18 years or older, able to provide written informed consent and able to understand and willing to comply with the requirements of the ...
... consent. Age 18 years or older at the time of informed consent. ECOG performance status of 0 or 1. Adequate bone marrow, renal, hepatic, pulmonary and ...
Provided a signed written informed consent form. Females of child-bearing potential and males participating in the study must agree to use at least 2 ...
Ability to give informed consent. If the patient is unable to give informed consent as a result of death or physical incapacity, then informed assent from next ...
Each clinical trial requires informed consent from the participant. This consent ensures that you understand key facts and potential risks about the research ...
Willing and able to give written informed consent and adhere to protocol requirements. 3. Patient has a history of multiple myeloma with relapsed and ...
Provide written informed consent. Male or female ages 18 or older. Evidence of cancer of the colon or rectum that is metastatic to the liver. NOTE: patients ...
Male or female subjects, 18-75 years of age at time of Screening who provide written informed consent prior to initiation of any study procedure.
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