drugset / Trial / NCT07188207

Rectal Misoprostol for Reducing Blood Loss in Elective Cesarean Section

NCT07188207

Not yet recruiting 282 enrolled Assiut University
RandomizedParallel-groupTriple-blindPrevention

Summary

This randomized controlled trial aims to evaluate the efficacy of adding preoperative rectal misoprostol to standard oxytocin for reducing intraoperative and postoperative blood loss in women undergoing elective cesarean section. Misoprostol is a prostaglandin E1 analogue that is inexpensive, heat-stable, and effective as a uterotonic agent. The study will compare outcomes between two groups: women receiving oxytocin alone and women receiving oxytocin plus rectal misoprostol. The primary outcome is the reduction of blood loss during and after surgery. Secondary outcomes include changes in hemoglobin levels, need for additional uterotonics, maternal safety, and overall recovery.

Timeline

Start
2025-10-01
Primary completion
2026-10-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Background Oxytocin Peptide 20 iu Intravenous

Indications

No indication recorded.