# Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours

> **NCT03045939** · NA · UNKNOWN · sponsor: **Bnai Zion Medical Center** · enrollment: 200 (estimated)

## Conditions studied

- Induction of Labor
- Unfavorable Cervix

## Interventions

- **DEVICE:** cervical ripening device

## Key facts

- **NCT ID:** NCT03045939
- **Lead sponsor:** Bnai Zion Medical Center
- **Sponsor class:** OTHER_GOV
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2017-03-01
- **Primary completion:** 2019-02-01
- **Final completion:** 2019-03-01
- **Target enrollment:** 200 (ESTIMATED)
- **Last updated:** 2019-03-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03045939

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03045939, "Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT03045939. Licensed CC0.

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