A randomized control trial on vasovagal reaction prevention strategies in whole blood donors
Not Applicable
Completed
- Registration Number
- CTRI/2021/01/030249
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 4458
Inclusion Criteria
1. Donor eligible according to the Departmental SOP and recent DCA amendment
2. Donors of age group �18 to 65 years
3. Both male and female donors
4. All first-time blood donors and
5. All repeat blood donors
Exclusion Criteria
1. Repeat donors with more than 3 previous donations within 2 years
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of VVR in intervention group compared to the non-intervention group.Timepoint: Outcomes will be assessed immediately post donation and after one week.
- Secondary Outcome Measures
Name Time Method Effectiveness of VVR prevention strategiesTimepoint: at the end of the study <br/ ><br>