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NCT01279343 · ClinicalTrials.gov registry record · NA
Cervical Foley Plus Vaginal Misoprostol for Labor Induction
A NA study, sponsored by Washington University School of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 123
- Enrollment target
NCT01279343: Completed NA study, sponsored by Washington University School of Medicine.
NCT01279343 is a NA study that has completed, run by Washington University School of Medicine. The registered enrollment target is 123 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01279343, a NA study, has completed, sponsored by Washington University School of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 123 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the efficacy of the combination of the supracervical foley bulb and vaginal misoprostol to vaginal misoprostol alone for labor induction. We hypothesize that use of the foley bulb plus vaginal misoprostol will result in shorter induction to delivery time.
Interventions
- DEVICE Foley bulb
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 123 participants |
| Start Date | 2011-01 |
| Est. Completion | 2014-03 |
| Phase | NA |
What the finished NCT01279343 record still lists
NCT01279343 is an interventional study that assigns participants to a tested intervention. The registered 123 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).
The record links to 0 conditions, and to 1 intervention - of which Foley bulb is the first listed.
NCT01279343 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01279343 about?
NCT01279343 is a clinical study titled "Cervical Foley Plus Vaginal Misoprostol for Labor Induction". The purpose of this study is to compare the efficacy of the combination of the supracervical foley bulb and vaginal misoprostol to vaginal misoprostol alone for labor induction. We hypothesize that use of the foley bulb plus vaginal misoprostol will result in shorter induction to delivery time.
What is the current status of trial NCT01279343?
This trial is currently completed. It is a NA study. The enrollment target is 123 participants. The study started on 2011-01. Estimated completion is 2014-03.
What interventions are being tested in trial NCT01279343?
The interventions under investigation include: Foley bulb (DEVICE).
Who is sponsoring clinical trial NCT01279343?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01279343's enrollment target sits among peer trials
123 762nd of 2000 higher than 1,239 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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