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NCT00325026 · ClinicalTrials.gov registry record · Phase 2
Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation
A Phase 2 study of Premature Birth and Cervical Ripening, sponsored by University of Florida.
- Completed
- Registry status
- Phase 2
- Development phase
- 130
- Enrollment target
- 1
- Study location
NCT00325026 is a Phase 2 study of Premature Birth and Cervical Ripening that has completed, run by University of Florida. The registered enrollment target is 130 participants, below the 391-participant average among 38 other Premature Birth trials with a reported enrollment target (67% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00325026, a Phase 2 study of Premature Birth and Cervical Ripening, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 130 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare the time to delivery of two different cervical ripening methods on the preterm gestation.
Conditions Studied
Interventions
- DRUG Misoprostol
- DEVICE Foley bulb
Study Locations (1)
Florida
- Shands Hospital at the University of Florida - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 130 participants |
| Start Date | 2005-04 |
| Est. Completion | 2007-04 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00325026
The ClinicalTrials.gov registry entry for NCT00325026 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 391-participant average among 38 other Premature Birth trials with a reported enrollment target (67% lower). The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Premature Birth appearing as the primary indexed condition, and to 2 interventions - of which Misoprostol is the first listed.
NCT00325026 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT00325026 about?
NCT00325026 is a clinical study titled "Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation". The purpose of this study is to compare the time to delivery of two different cervical ripening methods on the preterm gestation.
What is the current status of trial NCT00325026?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 130 participants. The study started on 2005-04. Estimated completion is 2007-04.
What conditions does trial NCT00325026 study?
This clinical trial studies the following conditions: Premature Birth, Cervical Ripening.
What interventions are being tested in trial NCT00325026?
The interventions under investigation include: Misoprostol (DRUG), Foley bulb (DEVICE).
Who is sponsoring clinical trial NCT00325026?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00325026 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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