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NCT01139801 · ClinicalTrials.gov registry record · NA
Cervical Ripening for Induction of Labor: Misoprostol Versus Oxytocin in Conjunction With Foley Balloon
A NA study, sponsored by Aultman Health Foundation.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT01139801: Completed NA study, sponsored by Aultman Health Foundation.
NCT01139801 is a NA study that has completed, run by Aultman Health Foundation. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01139801, a NA study, has completed, sponsored by Aultman Health Foundation.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to specifically investigate the efficacy of an alternative pharmacologic cervical ripening agent, misoprostol, versus the standard oxytocin, as an adjunct to Foley balloon for induction of the unfavorable cervix.
Primary Outcome
To assess effectiveness of misoprostol used in conjunction with Foley balloon versus the standard oxytocin regimen in regards to induction times
Interventions
- DRUG Oxytocin
- DRUG Misoprostol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2009-09 |
| Est. Completion | 2010-03 |
| Phase | NA |
What the finished NCT01139801 record still lists
NCT01139801 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Oxytocin is the first listed.
NCT01139801 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01139801 about?
NCT01139801 is a clinical study titled "Cervical Ripening for Induction of Labor: Misoprostol Versus Oxytocin in Conjunction With Foley Balloon". The purpose of this study is to specifically investigate the efficacy of an alternative pharmacologic cervical ripening agent, misoprostol, versus the standard oxytocin, as an adjunct to Foley balloon for induction of the unfavorable cervix.
What is the current status of trial NCT01139801?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2009-09. Estimated completion is 2010-03.
What interventions are being tested in trial NCT01139801?
The interventions under investigation include: Oxytocin (DRUG), Misoprostol (DRUG).
Who is sponsoring clinical trial NCT01139801?
This trial is sponsored by Aultman Health Foundation, which has 12 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01139801's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 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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