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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 is a NA study that has completed, run by Washington University School of Medicine. The registered enrollment target is 123 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01279343
The ClinicalTrials.gov registry entry for NCT01279343 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 123 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Foley bulb is the first listed.
NCT01279343 reports 0 study locations.
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.
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