# A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor

> **NCT02777190** · PHASE4 · TERMINATED · sponsor: **Milton S. Hershey Medical Center** · enrollment: 34 (actual)

## Conditions studied

- Labor; Forced or Induced, Affecting Fetus or Newborn
- Pregnancy

## Interventions

- **DRUG:** Misoprostol

## Key facts

- **NCT ID:** NCT02777190
- **Lead sponsor:** Milton S. Hershey Medical Center
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2017-11-01
- **Primary completion:** 2019-04-23
- **Final completion:** 2019-04-23
- **Target enrollment:** 34 (ACTUAL)
- **Why stopped:** Insufficient research staff to recruit and complete study
- **Last updated:** 2022-10-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02777190

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02777190, "A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT02777190. Licensed CC0.

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