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NCT00290199 · ClinicalTrials.gov registry record · NA
Foley Catheter for Labor Induction in Women With Term and Near Term Membrane Rupture
A NA study, sponsored by University of Alabama at Birmingham.
- Terminated
- Registry status
- NA
- Development phase
- 169
- Enrollment target
NCT00290199 is a NA study that was terminated before completion, run by University of Alabama at Birmingham. The registered enrollment target is 169 participants.
The verdict
NCT00290199, a NA study, was terminated before completion, sponsored by University of Alabama at Birmingham.
- TERMINATED
- Registry status
- NA
- Development phase
- 169 participants
- Enrollment target
Study Summary
In women undergoing labor induction for membrane rupture at or near term, we are investigating the addition of a foley catheter placed in the cervix to standard therapy (oxytocin administration) to decrease the time from the start of the induction to delivery.
Interventions
- DEVICE Transcervical Foley catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 169 participants |
| Start Date | 2005-12 |
| Est. Completion | 2008-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00290199
The ClinicalTrials.gov registry entry for NCT00290199 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 169 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Transcervical Foley catheter is the first listed.
NCT00290199 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00290199 about?
NCT00290199 is a clinical study titled "Foley Catheter for Labor Induction in Women With Term and Near Term Membrane Rupture". In women undergoing labor induction for membrane rupture at or near term, we are investigating the addition of a foley catheter placed in the cervix to standard therapy (oxytocin administration) to decrease the time from the start of the induction to delivery.
What is the current status of trial NCT00290199?
This trial is currently terminated. It is a NA study. The enrollment target is 169 participants. The study started on 2005-12. Estimated completion is 2008-05.
What interventions are being tested in trial NCT00290199?
The interventions under investigation include: Transcervical Foley catheter (DEVICE).
Who is sponsoring clinical trial NCT00290199?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
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