# Comparison Between Rectal & Sublingual Misoprostol Before Caesarian Section To Reduce Intra & Post-Operative Blood Loss

> **NCT02083107** · PHASE2,PHASE3 · COMPLETED · sponsor: **Ain Shams University** · enrollment: 636 (actual)

## Conditions studied

- Postpartum Hemorrhage

## Interventions

- **DRUG:** Misoprostol
- **OTHER:** Placebo

## Key facts

- **NCT ID:** NCT02083107
- **Lead sponsor:** Ain Shams University
- **Sponsor class:** OTHER
- **Phase:** PHASE2,PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-02
- **Primary completion:** 2014-02
- **Final completion:** 2014-02
- **Target enrollment:** 636 (ACTUAL)
- **Last updated:** 2015-12-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02083107

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02083107, "Comparison Between Rectal & Sublingual Misoprostol Before Caesarian Section To Reduce Intra & Post-Operative Blood Loss". Retrieved via AI Analytics 2026-06-04 from https://api.ai-analytics.org/clinical/NCT02083107. Licensed CC0.

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