# Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Women Delivered Only by Cesarean Delivery

> **NCT04080349** · PHASE4 · UNKNOWN · sponsor: **Cairo University** · enrollment: 300 (estimated)

## Conditions studied

- IUD Pain

## Interventions

- **DRUG:** Dinoprostone 3 mg
- **DRUG:** Misoprostol 200Mcg Tab
- **DRUG:** placebo

## Key facts

- **NCT ID:** NCT04080349
- **Lead sponsor:** Cairo University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-09-10
- **Primary completion:** 2019-11-30
- **Final completion:** 2019-12-05
- **Target enrollment:** 300 (ESTIMATED)
- **Last updated:** 2019-09-06


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04080349

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04080349, "Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Women Delivered Only by Cesarean Delivery". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT04080349. Licensed CC0.

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