Search Results 851-860 of 21218 for Informed consent
Subject must be able to understand and provide informed consent. · Age ≥ 18 years of age at the time of study entry. · Recipients of non- Human Leukocyte Antigen ...
Provide written informed consent; Willing and able to comply with all aspects of the protocol. Exclusion Criteria. Any history of arterial or venous thrombosis ...
... informed consent. Eligibility last updated 7/26/23. Questions regarding updates should be directed to the study team contact. Participating Mayo Clinic ...
Participants with certain physical and mental disabilities that might interfere with their ability to give informed consent, cooperate with the researcher, or ...
* Provide written informed consent * Willing to return to enrolling institution for follow-up (during the Active Monitoring Phase and the Event Monitoring ...
Patient or caregiver willing and able to provide written informed consent. Primary language of English or Spanish for patients and their caregiver. Negative ...
... informed consent until 30 days after the last administration of study drug. Females of childbearing potential should have a negative serum pregnancy test ...
Any major surgery, or significant post-operative sequelae, within 1 month prior to informed consent or planned during the trial. Pregnant, lactating, or ...
Able and willing to provide written informed consent. Exclusion Criteria: Failure to meet 21 CFR 1271 donor eligibility criteria based on responses to a ...
Provide written informed consent; Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study); Willing to ...
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