# Oral Misoprostol for Cervical Priming Before Hysteroscopy

> **NCT02159911** · — · COMPLETED · sponsor: **Saint-Joseph University** · enrollment: 84 (actual)

## Conditions studied

- Cervical Laceration
- Adverse Effects

## Interventions

- **DRUG:** Misoprostol administered orally one hour before surgery

## Key facts

- **NCT ID:** NCT02159911
- **Lead sponsor:** Saint-Joseph University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2004-06
- **Primary completion:** 2004-11
- **Final completion:** 2004-11
- **Target enrollment:** 84 (ACTUAL)
- **Last updated:** 2014-06-10


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02159911

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02159911, "Oral Misoprostol for Cervical Priming Before Hysteroscopy". Retrieved via AI Analytics 2026-06-05 from https://api.ai-analytics.org/clinical/NCT02159911. Licensed CC0.

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