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NCT03976037 · ClinicalTrials.gov registry record · Early Phase 1
Buccal Versus Vaginal Misoprostol In Combination With Foley Bulb
A Early Phase 1 study, sponsored by Christiana Care Health Services.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 216
- Enrollment target
NCT03976037: Completed Early Phase 1 study, sponsored by Christiana Care Health Services.
NCT03976037 is a Early Phase 1 study that has completed, run by Christiana Care Health Services. The registered enrollment target is 216 participants, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (308% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03976037, a Early Phase 1 study, has completed, sponsored by Christiana Care Health Services.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 216 participants
- Enrollment target
Study Summary
Combined misoprostol and Foley bulb catheter has been shown to be an effective induction method. However, optimal route of administration for misoprostol has not been established. Therefore, the purpose of this study is to compare the effectiveness and safety of combination buccal miso-foley to combination vaginal miso-foley for third trimester cervical ripening and induction of labor.
Primary Outcome
as time from initiation of induction method to delivery time, regardless of mode of delivery.
Interventions
- DRUG Misoprostol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 216 participants |
| Start Date | 2019-06-04 |
| Est. Completion | 2021-02-01 |
| Phase | Early Phase 1 |
What the finished NCT03976037 record still lists
NCT03976037 is an interventional study that assigns participants to a tested intervention. The registered 216 participants enrollment target is mid-sized for trials with a published cap, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (308% higher).
The record links to 0 conditions, and to 1 intervention - of which Misoprostol is the first listed.
NCT03976037 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03976037 about?
NCT03976037 is a clinical study titled "Buccal Versus Vaginal Misoprostol In Combination With Foley Bulb". Combined misoprostol and Foley bulb catheter has been shown to be an effective induction method. However, optimal route of administration for misoprostol has not been established. Therefore, the purpose of this study is to compare the effectiveness and safety of combination buccal miso-foley to com...
What is the current status of trial NCT03976037?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 216 participants. The study started on 2019-06-04. Estimated completion is 2021-02-01.
What interventions are being tested in trial NCT03976037?
The interventions under investigation include: Misoprostol (DRUG).
Who is sponsoring clinical trial NCT03976037?
This trial is sponsored by Christiana Care Health Services, which has 82 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03976037's enrollment target sits among peer trials
216 57th of 2000 higher than 1,944 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 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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