Search Results 1001-1010 of 21160 for Informed consent
In case of inclusion of such patients, informed consent would need to be administered according to ICH GCP sections 1.37 and/or 4.8.12, as applicable.
Informed consent to collect this information will be done at their surgical evaluation visit; If not able to be consented at this visit, they will be called ...
Inability or unwillingness of individual or legal guardian/representative to give written informed consent. Participating Mayo Clinic locations. Study ...
Medical or psychiatric conditions that compromise the subject's ability to give informed consent or to complete the protocol or a history of non-compliance ...
... informed consent prior to initiation of any study specific activities/procedures. Subject is an adult ≥ 18 years old at the time of signing the informed ...
Patient must have a signed study informed consent prior to entering the study. Histologically confirmed MM prior to enrollment and randomization. At least 1 ...
Able to read and understand informed consent form. Exclusion Criteria: Non-English speaking women; First-case of the day gynecological surgery patients ...
Participation eligibility · Adult male or female ≥ 18 years of age at the time of signing the informed consent form · Clinical diagnosis of acquired TTP (initial ...
Inability to provide informed consent AND absence of a surrogate decision maker. Participants will not be excluded if they have conditions such as ...
Inability to provide informed consent to participate in the study. Note: Other protocol defined Inclusion/Exclusion Criteria may apply. Eligibility last ...
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