Comparison of two informed consent processes
Not Applicable
- Registration Number
- CTRI/2015/05/005736
- Lead Sponsor
- Department of Clinical Pharmacology Seth GSMCandKEMHospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
participation and completion of follow ups in rabies monoclonal antibody study conducted in the department.
willing to give informed consent
Exclusion Criteria
participants who withdrew consent or discontinued from the rabies monoclonal antibody study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method