# Prehospital Cervical Ripening Before Induction and the Maternal Experience

> **NCT01641601** · NA · TERMINATED · sponsor: **University of California, San Francisco** · enrollment: 8 (actual)

## Conditions studied

- Labor, Induced
- Cervical Ripening

## Interventions

- **DEVICE:** Outpatient transcervical Foley balloon

## Key facts

- **NCT ID:** NCT01641601
- **Lead sponsor:** University of California, San Francisco
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2012-07
- **Primary completion:** 2015-07
- **Final completion:** 2015-07
- **Target enrollment:** 8 (ACTUAL)
- **Why stopped:** Inadequate enrollment. Key study personnel transitioned to a different role.
- **Last updated:** 2020-08-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01641601

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01641601, "Prehospital Cervical Ripening Before Induction and the Maternal Experience". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01641601. Licensed CC0.

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