nderstanding the type of delayed adverse reactions in whole blood donors
Not Applicable
- Registration Number
- CTRI/2023/02/050015
- Lead Sponsor
- Sowmya Nayak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All blood donors who have undergone whole blood donation with an age group between 18 to 65 years
Exclusion Criteria
Donors under medication
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Prevalence of commonest delayed donor reaction among voluntary blood donorsTimepoint: One year
- Secondary Outcome Measures
Name Time Method Validated Interview ScriptTimepoint: 6 months