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NCT03111316 · ClinicalTrials.gov registry record · NA
Foley Catheter Compared to the Foley Catheter Alone for Cervical Ripening
A NA study of Cervical Ripening and Induction of Labor, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT03111316 is a NA study of Cervical Ripening and Induction of Labor that has completed, run by University of Oklahoma. The registered enrollment target is 100 participants, below the 458-participant average among 8 other Cervical Ripening trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03111316, a NA study of Cervical Ripening and Induction of Labor, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
In term women presenting for labor induction, combined use of the controlled release dinoprostone vaginal insert and Foley catheter for cervical ripening will decrease the median time from induction to vaginal delivery by at least four hours compared to the Foley catheter alone.
Conditions Studied
Interventions
- DEVICE Foley Catheter
- DRUG Cervidil 10 MG Vaginal Insert
Study Locations (1)
Oklahoma
- The University of Oklahoma Health Sciences Center - Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2017-04-09 |
| Est. Completion | 2020-07-24 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03111316
The ClinicalTrials.gov registry entry for NCT03111316 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 458-participant average among 8 other Cervical Ripening trials with a reported enrollment target (78% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Cervical Ripening appearing as the primary indexed condition, and to 2 interventions - of which Foley Catheter is the first listed.
NCT03111316 reports 1 study location spanning 1 distinct geographic area - top geographies include Oklahoma.
Frequently Asked Questions
What is clinical trial NCT03111316 about?
NCT03111316 is a clinical study titled "Foley Catheter Compared to the Foley Catheter Alone for Cervical Ripening". In term women presenting for labor induction, combined use of the controlled release dinoprostone vaginal insert and Foley catheter for cervical ripening will decrease the median time from induction to vaginal delivery by at least four hours compared to the Foley catheter alone.
What is the current status of trial NCT03111316?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2017-04-09. Estimated completion is 2020-07-24.
What conditions does trial NCT03111316 study?
This clinical trial studies the following conditions: Cervical Ripening, Induction of Labor.
What interventions are being tested in trial NCT03111316?
The interventions under investigation include: Foley Catheter (DEVICE), Cervidil 10 MG Vaginal Insert (DRUG).
Who is sponsoring clinical trial NCT03111316?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03111316 being conducted?
This trial has 1 study location across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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