A Comparative Study Between Rectal and Intrauterine Misoprostol Administration in the Reduction of Blood Loss During and After Elective Cesarean Delivery in Low Risk Women
Clinical trial NCT07728084 · COMPLETED
Trial details
- NCT number
- NCT07728084
- Sponsor
- Cairo University
- Status
- COMPLETED
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2025-01-13
- Primary completion
- 2026-04-25
- Enrollment
- 140
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