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NCT03665688 · ClinicalTrials.gov registry record · NA
Comparing Outpatient to Inpatient Cervical Ripening Using Dilapan-S®
A NA study, sponsored by The University of Texas Medical Branch, Galveston.
- Completed
- Registry status
- NA
- Development phase
- 338
- Enrollment target
NCT03665688 is a NA study that has completed, run by The University of Texas Medical Branch, Galveston. The registered enrollment target is 338 participants.
The verdict
NCT03665688, a NA study, has completed, sponsored by The University of Texas Medical Branch, Galveston.
- COMPLETED
- Registry status
- NA
- Development phase
- 338 participants
- Enrollment target
Study Summary
The target population for our study is women who present for induction of labor. If there is a decision by the obstetrical team to place a mechanical dilator for cervical ripening, the obstetrical team will notify the research staff so that the patient may be screened for the study. If the subject is eligible for the trial, written informed consent will be obtained by person-to-person contact. The PI, study coordinator, or a collaborator will be responsible for the informed consent procedure. After informed consent is obtained and Dilapan-S is placed, the patient will be randomized to the Outpatient or the Inpatient group.
Interventions
- DEVICE Outpatient Dilapan-S
- DEVICE Inpatient Dilapan-S
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 338 participants |
| Start Date | 2018-11-07 |
| Est. Completion | 2021-11-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03665688
The ClinicalTrials.gov registry entry for NCT03665688 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 338 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 Outpatient Dilapan-S is the first listed.
NCT03665688 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03665688 about?
NCT03665688 is a clinical study titled "Comparing Outpatient to Inpatient Cervical Ripening Using Dilapan-S®". The target population for our study is women who present for induction of labor. If there is a decision by the obstetrical team to place a mechanical dilator for cervical ripening, the obstetrical team will notify the research staff so that the patient may be screened for the study. If the subject i...
What is the current status of trial NCT03665688?
This trial is currently completed. It is a NA study. The enrollment target is 338 participants. The study started on 2018-11-07. Estimated completion is 2021-11-05.
What interventions are being tested in trial NCT03665688?
The interventions under investigation include: Outpatient Dilapan-S (DEVICE), Inpatient Dilapan-S (DEVICE).
Who is sponsoring clinical trial NCT03665688?
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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