To give tranexamic acid in reducing postpartum blood loss in vaginal deliveries
Phase 2
- Registration Number
- CTRI/2024/04/066348
- Lead Sponsor
- DR SN MEDICAL COLLEGE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
prmigravida or secondary gravida
37 to 42 weeks of gestation
admitted in active labour
normotensive
cephalic presentation
Exclusion Criteria
All other patients not fulfilling the inclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To quantify the mean 2hour postpartum blood lossTimepoint: from delivery to 2 hour postpartum
- Secondary Outcome Measures
Name Time Method To see if any other intervention needed after delivery & to compare the need of blood transfusion & to see the potential adverse effects of tranexamic acid. <br/ ><br>Timepoint: from delivery till patient discharged.