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NCT03086967 · ClinicalTrials.gov registry record · NA
Cervical Ripening With a Double-lumen Balloon Catheter for Six Versus Twelve Hours
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 204
- Enrollment target
NCT03086967: Completed NA study, sponsored by Wake Forest University Health Sciences.
NCT03086967 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 204 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03086967, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 204 participants
- Enrollment target
Study Summary
The Foley catheter is a safe, effective method for cervical ripening. Limited data exists to indicate ideal time of placement for optimal cervical ripening prior to induction. The proposed study is a randomized control trial to determine if shortening placement from 12 to 6 hours of foley catheter can decrease time from start of induction to delivery. The prediction is that shortening foley bulb placement will result in shorter induction times, increased patient satisfaction and decreased length of stay on labor and delivery with secondary decreased medical costs.
Primary Outcome
Time in hours to delivery following use of foley catheter
Interventions
- DEVICE Double-lumen balloon catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2013-06 |
| Est. Completion | 2016-02 |
| Phase | NA |
What the finished NCT03086967 record still lists
NCT03086967 is an interventional study that assigns participants to a tested intervention. The registered 204 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 (85% lower).
The record links to 0 conditions, and to 1 intervention - of which Double-lumen balloon catheter is the first listed.
NCT03086967 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03086967 about?
NCT03086967 is a clinical study titled "Cervical Ripening With a Double-lumen Balloon Catheter for Six Versus Twelve Hours". The Foley catheter is a safe, effective method for cervical ripening. Limited data exists to indicate ideal time of placement for optimal cervical ripening prior to induction. The proposed study is a randomized control trial to determine if shortening placement from 12 to 6 hours of foley catheter c...
What is the current status of trial NCT03086967?
This trial is currently completed. It is a NA study. The enrollment target is 204 participants. The study started on 2013-06. Estimated completion is 2016-02.
What interventions are being tested in trial NCT03086967?
The interventions under investigation include: Double-lumen balloon catheter (DEVICE).
Who is sponsoring clinical trial NCT03086967?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03086967's enrollment target sits among peer trials
204 500th of 2000 higher than 1,497 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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