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NCT01641601 · ClinicalTrials.gov registry record · NA
Prehospital Cervical Ripening Before Induction and the Maternal Experience
A NA study, sponsored by University of California, San Francisco.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT01641601: Clinical Trial NA study, sponsored by University of California, San Francisco.
NCT01641601 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01641601, a NA study, was terminated before completion, sponsored by University of California, San Francisco.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
This is a randomized study evaluating the impact of pre-hospital cervical ripening with a transcervical Foley balloon before labor induction in full-term pregnancies on the length of inpatient labor induction and maternal satisfaction with the labor induction process. The investigators hypothesize that women who receive pre-hospital cervical ripening will have a shorter duration of inpatient labor induction as compared to women without pre-hospital cervical ripening.
Primary Outcome
Time from admission to the hospital until delivery
Interventions
- DEVICE Outpatient transcervical Foley balloon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2012-07 |
| Est. Completion | 2015-07 |
| Phase | NA |
Why NCT01641601 stopped before completion
NCT01641601 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Outpatient transcervical Foley balloon is the first listed.
NCT01641601 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01641601 about?
NCT01641601 is a clinical study titled "Prehospital Cervical Ripening Before Induction and the Maternal Experience". This is a randomized study evaluating the impact of pre-hospital cervical ripening with a transcervical Foley balloon before labor induction in full-term pregnancies on the length of inpatient labor induction and maternal satisfaction with the labor induction process. The investigators hypothesize t...
What is the current status of trial NCT01641601?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2012-07. Estimated completion is 2015-07.
What interventions are being tested in trial NCT01641601?
The interventions under investigation include: Outpatient transcervical Foley balloon (DEVICE).
Who is sponsoring clinical trial NCT01641601?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01641601's enrollment target sits among peer trials
8 1976th of 2000 higher than 19 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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