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NCT02899689 · ClinicalTrials.gov registry record · NA
Induction of Labor in Women With Unfavorable Cervix: Dilapan Versus Foley Bulb
A NA study, sponsored by The University of Texas Medical Branch, Galveston.
- Completed
- Registry status
- NA
- Development phase
- 419
- Enrollment target
NCT02899689 is a NA study that has completed, run by The University of Texas Medical Branch, Galveston. The registered enrollment target is 419 participants.
The verdict
NCT02899689, a NA study, has completed, sponsored by The University of Texas Medical Branch, Galveston.
- COMPLETED
- Registry status
- NA
- Development phase
- 419 participants
- Enrollment target
Study Summary
Women undergoing mechanical cervical ripening for labor induction will be randomized to Dilapan-S® versus Foley bulb. The investigators hypothesized that osmotic cervical dilators (Dilapan-S®) are as effective as Foley bulb catheter in rates of vaginal delivery.
Interventions
- DEVICE Foley Catheter
- DEVICE Dilapan
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 419 participants |
| Start Date | 2016-09 |
| Est. Completion | 2018-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02899689
The ClinicalTrials.gov registry entry for NCT02899689 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 419 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Medical Branch, Galveston, which has 203 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Foley Catheter is the first listed.
NCT02899689 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02899689 about?
NCT02899689 is a clinical study titled "Induction of Labor in Women With Unfavorable Cervix: Dilapan Versus Foley Bulb". Women undergoing mechanical cervical ripening for labor induction will be randomized to Dilapan-S® versus Foley bulb. The investigators hypothesized that osmotic cervical dilators (Dilapan-S®) are as effective as Foley bulb catheter in rates of vaginal delivery.
What is the current status of trial NCT02899689?
This trial is currently completed. It is a NA study. The enrollment target is 419 participants. The study started on 2016-09. Estimated completion is 2018-02.
What interventions are being tested in trial NCT02899689?
The interventions under investigation include: Foley Catheter (DEVICE), Dilapan (DEVICE).
Who is sponsoring clinical trial NCT02899689?
This trial is sponsored by The University of Texas Medical Branch, Galveston, which has 203 total clinical trials registered on ClinicalTrials.gov.
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