Search Results 1671-1680 of 20644 for Informed consent
Inability to provide informed consent. Age under 18 years. Participating Mayo Clinic locations. Study statuses change often. Please contact the study team ...
... informed consent, and subject provides written assent, as required by the Mayo Clinic Institutional Review Board (IRB) policy involving human subjects. In ...
Informed consent obtained before any study-related activities. · Male or female. · Age ≥ 18 to < 85 years at the time of signing informed consent. · Have an ...
Participation eligibility · Patients ≥ 18 to ≤ 80 years (at date of signing the informed consent form [ICF]), but at least of legal age in the given country.
Subject is able to provide written informed consent and is willing and able to complete study procedures. Subject must meet criteria for either ATTR cardiac ...
Be willing and able to provide written informed consent/assent for the trial. Be ≥ 18 years of age on day of signing informed consent. Have received 1-5 ...
Unwilling or unable to obtain informed consent from the participant or substitute decision maker. Revascularization of coronary artery disease performed in ...
... informed consent form and assent, if applicable. Male and female patients ... Male and female patients aged ≥ 2 and ≤ 17 years at the time of informed consent ...
Signed and informed consent to participant in this study; Willing to participate in associated correlative science biomarker study; Serum creatinine < 1.5 x ...
Able to provide a valid informed consent to be in the study (self or their authorized legally accepted representative). The approved consent form must be ...
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