# 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

> **NCT07728084** · NA · COMPLETED · sponsor: **Cairo University** · enrollment: 140 (actual)

## Conditions studied

- Postpartum Hemorrhage， Cesarean Section

## Interventions

- **DRUG:** Misoprostol Tabets
- **DRUG:** Misoprostol Tabets

## Key facts

- **NCT ID:** NCT07728084
- **Lead sponsor:** Cairo University
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2025-01-13
- **Primary completion:** 2026-04-25
- **Final completion:** 2026-06-29
- **Target enrollment:** 140 (ACTUAL)
- **Last updated:** 2026-07-27


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07728084

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07728084, "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". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07728084. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*