Developing and sharing techniques in which The informed consent process, the process by which a potential research participant learns about and understands the purpose, benefits, and potential risks and then agrees to participate in the research in low- and middle- income countries
Not Applicable
- Registration Number
- CTRI/2020/01/022847
- Lead Sponsor
- Seth GSMC KEM Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other (Terminated)
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
One ongoing RCT in the Department of Clinical Pharmacology will be selected randomly and participants who go through the informed consent process will be included
Exclusion Criteria
Sponsor of the RCT denies permission
The potential participant of the chosen RCT who is going through the informed consent process denies consent for this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method