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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 is a NA study that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 200 participants.
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
Interventions
- DEVICE Foley bulb
- DEVICE misoprostol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2015-09 |
| Est. Completion | 2016-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02566005
The ClinicalTrials.gov registry entry for NCT02566005 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Foley bulb is the first listed.
NCT02566005 reports 0 study locations.
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.
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