A clinical trial to study the effect of drug tranexamic acid in addition to oxytocin in reducing blood loss after vaginal delivery
Phase 4
- Conditions
- Health Condition 1: O720- Third-stage hemorrhage
- Registration Number
- CTRI/2023/09/057612
- Lead Sponsor
- PT J N M Medical College Raipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
WOMEN PLANNED FOR VAGINAL DELIVERY
Exclusion Criteria
AGE < 18 YEARS
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood loss after vaginal deliveryTimepoint: Within 1 hour after vaginal delivery
- Secondary Outcome Measures
Name Time Method Haemoglobin levelTimepoint: After 24 hours of vaginal delivery