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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 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 204 participants.
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.
Interventions
- DEVICE Double-lumen balloon catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2013-06 |
| Est. Completion | 2016-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03086967
The ClinicalTrials.gov registry entry for NCT03086967 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 204 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Double-lumen balloon catheter is the first listed.
NCT03086967 reports 0 study locations.
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.
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