Search Results 891-900 of 21234 for Informed consent
Before patient registration, written informed consent must be obtained according to ICH/GCP, and national/local regulations. Collection of left-over FFPE ...
Informed consent will be obtained for the two pituitary specimens under this present protocol. Population: Retrospective case series of patients who ...
Written informed consent must be obtained and documented. Exclusion Criteria: Diagnosis of Crohn's disease or indeterminate colitis. An active, serious ...
Subject or legally authorized representative is willing and able to provide written informed consent,. 2. Subject is 18 years or older,. 3. Subject is ...
Signed informed consent. Exclusion Criteria: Biochemical relapse alone without clinically suspicious (i.e. no suspicious lesion on MRI of the prostatic bed) ...
Sufficient cognitive function to understand the expectations of the study and provide informed consent. Exclusion Criteria: Admitted from another hospital ...
Participants are able and willing to provide signed informed consent. Female patients of childbearing potential must have a negative pregnancy test result ...
Willing and able to provide informed consent to participate in the study at enrollment * and be followed at one of the participating MARS Consortium Sites ...
Unable to provide informed consent; Claustrophobia; Planning to move within 24 months of trial enrollment; Pregnant or breast-feeding. Participating Mayo Clinic ...
Signed informed consent. If taking pirfenidone or nintedanib, must be on stable dose for at least 6 weeks prior to enrollment visit. Confirmed rs3570920 TT ...
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