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NCT02777190 · ClinicalTrials.gov registry record · Phase 4
A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor
A Phase 4 study, sponsored by Milton S. Hershey Medical Center.
- Terminated
- Registry status
- Phase 4
- Development phase
- 34
- Enrollment target
NCT02777190 is a Phase 4 study that was terminated before completion, run by Milton S. Hershey Medical Center. The registered enrollment target is 34 participants.
The verdict
NCT02777190, a Phase 4 study, was terminated before completion, sponsored by Milton S. Hershey Medical Center.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 34 participants
- Enrollment target
Study Summary
The purpose of this study is to study if misoprostol administered orally is at least as effective as misoprostol administered vaginally for cervical ripening and the induction of labor. The main purpose is to show that oral misoprostol administration is non-inferior to vaginal misoprostol administration with respect to the time interval from misoprostol administration to onset of active phase of labor. The study is a non-inferiority, prospective randomized controlled trial comparing oral misoprostol given as 25 mcg every 2 hours versus vaginal misoprostol given as 25 mcg every 4 hours.
Interventions
- DRUG Misoprostol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 34 participants |
| Start Date | 2017-11-01 |
| Est. Completion | 2019-04-23 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02777190
The ClinicalTrials.gov registry entry for NCT02777190 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Milton S. Hershey Medical Center, which has 396 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Misoprostol is the first listed.
NCT02777190 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02777190 about?
NCT02777190 is a clinical study titled "A Comparison of Oral Misoprostol and Vaginal Misoprostol for Cervical Ripening and Induction of Labor". The purpose of this study is to study if misoprostol administered orally is at least as effective as misoprostol administered vaginally for cervical ripening and the induction of labor. The main purpose is to show that oral misoprostol administration is non-inferior to vaginal misoprostol administra...
What is the current status of trial NCT02777190?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 34 participants. The study started on 2017-11-01. Estimated completion is 2019-04-23.
What interventions are being tested in trial NCT02777190?
The interventions under investigation include: Misoprostol (DRUG).
Who is sponsoring clinical trial NCT02777190?
This trial is sponsored by Milton S. Hershey Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov.
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