CTRI/2021/03/032275
Not yet recruiting
Phase 4
To study efficay of sublingual Misoprostol vs intravenous Tranexamic acid in reducing amount of blood loss in full term pregnant women undergoing primary LSCS :A randomized control trial
Aarupadi Veedu Medical College and Hoppital0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: O94-O9A- Other obstetric conditions, not elsewhere classified
- Sponsor
- Aarupadi Veedu Medical College and Hoppital
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Full term women undergoing primary Cesarean Section at Aarupadi Veedu Medical College and Hospital who are willing to participate
Exclusion Criteria
- •1\)Previous Cesarean Section
- •2\)Induced/augmented labour
- •4\)chorioamnionitis
- •5\)antepartum hemorrhage
- •6\)pre term pregnancy
- •7\)overdistension\-multipregnancy,polyhydromnios
Outcomes
Primary Outcomes
Not specified
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