# Cervical Ripening With a Double-lumen Balloon Catheter for Six Versus Twelve Hours

> **NCT03086967** · NA · COMPLETED · sponsor: **Wake Forest University Health Sciences** · enrollment: 204 (actual)

## Conditions studied

- Induction of Labor Affected Fetus / Newborn

## Interventions

- **DEVICE:** Double-lumen balloon catheter

## Key facts

- **NCT ID:** NCT03086967
- **Lead sponsor:** Wake Forest University Health Sciences
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-06
- **Primary completion:** 2015-09
- **Final completion:** 2016-02
- **Target enrollment:** 204 (ACTUAL)
- **Last updated:** 2022-11-30


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03086967

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03086967, "Cervical Ripening With a Double-lumen Balloon Catheter for Six Versus Twelve Hours". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT03086967. Licensed CC0.

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