Search Results 1291-1300 of 21218 for Informed consent
Informed consent for the study participation obtained from participant or their legally authorized representatives. Exclusion Criteria: 1. Patients planned ...
Unable to provide informed consent. Less than 80% compliance with providing headache diary data during the run‐in phase (i.e., provides data on less than 80 ...
Patient and/or legal guardian is able to read, understand, and sign the informed consent. Where appropriate, assent will also be sought for patients < 18 ...
Informed consent for the study will be obtained from the patients or their surrogate. Participating Mayo Clinic locations. Study statuses change often. Please ...
Unable to provide informed consent; Use of chronic intermittent self-catheterization pre-operatively; Use of chronic prophylactic antibiotics; Use of ...
Patient has signed and dated informed consent. Patient has suitable anatomy for implant of the WiSE CRT System (e.g., adequate acoustic window, LV wall ...
Ability to provide informed consent; Ability to understand English. Exclusion Criteria: A medical contraindication that precludes SSRI or SNRI treatment ...
The participant and/or the participants' parent/legal guardian is willing and able to provide signed informed consent, and willing to be followed up to five ...
Adults over the age of 18-50 years and who are willing and able to give informed consent. No known diseases (i.e., cardiovascular, pulmonary, diabetes ...
Written informed consent must be provided. Exclusion Criteria. Subjects with AML in their first relapse following a remission >12 months in duration; Leukemic ...
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