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NCT02566005 · ClinicalTrials.gov registry record · NA
A Randomized Comparison of Transcervical Foley Bulb With Vaginal Misoprostol to Vaginal Misoprostol Alone for Induction of Labor
A NA study, sponsored by St. Luke's-Roosevelt Hospital Center.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT02566005: Completed NA study, sponsored by St. Luke's-Roosevelt Hospital Center.
NCT02566005 is a NA study that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02566005, a NA study, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study Summary
A randomized, prospective trial will be offered to women admitted to the Roosevelt Hospital labor floor for labor induction. The hypothesis is that the simultaneous use of a foley bulb together with vaginal misoprostol will result in shorter induction to delivery time compared with vaginal misoprostol alone
Primary Outcome
During labor from the start of the induction to the delivery
Interventions
- DEVICE Foley bulb
- DEVICE misoprostol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2015-09 |
| Est. Completion | 2016-07 |
| Phase | NA |
What the finished NCT02566005 record still lists
NCT02566005 is an interventional study that assigns participants to a tested intervention. The registered 200 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 (86% lower).
The record links to 0 conditions, and to 2 interventions - of which Foley bulb is the first listed.
NCT02566005 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02566005 about?
NCT02566005 is a clinical study titled "A Randomized Comparison of Transcervical Foley Bulb With Vaginal Misoprostol to Vaginal Misoprostol Alone for Induction of Labor". A randomized, prospective trial will be offered to women admitted to the Roosevelt Hospital labor floor for labor induction. The hypothesis is that the simultaneous use of a foley bulb together with vaginal misoprostol will result in shorter induction to delivery time compared with vaginal misoprost...
What is the current status of trial NCT02566005?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2015-09. Estimated completion is 2016-07.
What interventions are being tested in trial NCT02566005?
The interventions under investigation include: Foley bulb (DEVICE), misoprostol (DEVICE).
Who is sponsoring clinical trial NCT02566005?
This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02566005's enrollment target sits among peer trials
200 506th of 2000 higher than 1,434 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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