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NCT01641601 · ClinicalTrials.gov registry record · NA
Prehospital Cervical Ripening Before Induction and the Maternal Experience
A NA study, sponsored by University of California, San Francisco.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT01641601 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 8 participants.
The verdict
NCT01641601, a NA study, was terminated before completion, sponsored by University of California, San Francisco.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
This is a randomized study evaluating the impact of pre-hospital cervical ripening with a transcervical Foley balloon before labor induction in full-term pregnancies on the length of inpatient labor induction and maternal satisfaction with the labor induction process. The investigators hypothesize that women who receive pre-hospital cervical ripening will have a shorter duration of inpatient labor induction as compared to women without pre-hospital cervical ripening.
Interventions
- DEVICE Outpatient transcervical Foley balloon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2012-07 |
| Est. Completion | 2015-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01641601
The ClinicalTrials.gov registry entry for NCT01641601 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Outpatient transcervical Foley balloon is the first listed.
NCT01641601 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01641601 about?
NCT01641601 is a clinical study titled "Prehospital Cervical Ripening Before Induction and the Maternal Experience". This is a randomized study evaluating the impact of pre-hospital cervical ripening with a transcervical Foley balloon before labor induction in full-term pregnancies on the length of inpatient labor induction and maternal satisfaction with the labor induction process. The investigators hypothesize t...
What is the current status of trial NCT01641601?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2012-07. Estimated completion is 2015-07.
What interventions are being tested in trial NCT01641601?
The interventions under investigation include: Outpatient transcervical Foley balloon (DEVICE).
Who is sponsoring clinical trial NCT01641601?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
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