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NCT00366951 · ClinicalTrials.gov registry record · NA
A Randomized Study on Comparing the Efficacy of Foley Catheter and Extraamniotic Saline Infusion for Labor Induction
A NA study, sponsored by Rush University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT00366951 is a NA study that has completed, run by Rush University Medical Center. The registered enrollment target is 200 participants.
The verdict
NCT00366951, a NA study, has completed, sponsored by Rush University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study Summary
Our purpose was to compare the efficacy and safety of Foley catheter with oxytocin and extraamniotic saline infusion with oxytocin for induction of labor requiring cervical ripening.
Interventions
- PROCEDURE Foley catheter only
- PROCEDURE Extraamniotic saline infusion
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2004-04 |
| Est. Completion | 2005-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00366951
The ClinicalTrials.gov registry entry for NCT00366951 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rush University Medical Center, which has 320 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Foley catheter only is the first listed.
NCT00366951 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00366951 about?
NCT00366951 is a clinical study titled "A Randomized Study on Comparing the Efficacy of Foley Catheter and Extraamniotic Saline Infusion for Labor Induction". Our purpose was to compare the efficacy and safety of Foley catheter with oxytocin and extraamniotic saline infusion with oxytocin for induction of labor requiring cervical ripening.
What is the current status of trial NCT00366951?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2004-04. Estimated completion is 2005-11.
What interventions are being tested in trial NCT00366951?
The interventions under investigation include: Foley catheter only (PROCEDURE), Extraamniotic saline infusion (PROCEDURE).
Who is sponsoring clinical trial NCT00366951?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
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