Search Results 871-880 of 5147 for Informed consent
Patient is unable to provide informed consent. Patient has pre-existing respiratory condition. Participating Mayo Clinic locations. Study statuses change ...
De-identified clinical waste specimens from Mayo Clinic or outside facilities and/or appropriate tissues obtained with informed consent from patients with a ...
Signed written informed consent. 2. Male or female patients aged ≥ 18 years. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at ...
The purpose of this study is to obtain tissue, blood, saliva, and stool specimens and informed consent from ENT patients in order to build a freezer archive ...
Able to provide written informed consent for this long-term follow-up study 3. Able to comply with study requirements. Exclusion Criteria: 1. There are no ...
Written consent provided according to the IRB/EC defined and approved approvals for patients who are not able to provide independent, written informed consent.
- Signed informed consent prior to participation in the study. - Male or female participants aged 18 years and older on the day of signing informed consent - ...
Willing and able to provide written informed consent and privacy authorization for the release of personal health information. Males 21 years of age and ...
(4) Parent is able to provide informed consent. Exclusion criteria. (1) Do not read and speak English. (2) Has cognitive impairment. Participating Mayo Clinic ...
Willing and able to provide written informed consent or have a legally authorized representative (LAR) who will provide informed consent. Exclusion Criteria ...
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