Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation
Completed · Phase 2
Conditions studied: Premature Birth, Cervical Ripening
In brief
The purpose of this study is to compare the time to delivery of two different cervical ripening methods on the preterm gestation.
Key facts
- Study ID
- NCT00325026
- Run by
- University of Florida
- People needed
- 130
- Starts
- 2005-04-01
- Expected to finish
- 2007-04-01
- Last updated by the study team
- 2012-03-02
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- singleton gestation, gestational age 23-35 weeks, indication for induction
You may not qualify if…
- multiple gestation, non-cephalic presentation, previous uterine surgery, rupture of membranes, intrauterine fetal death
Where it is running
- Shands Hospital at the University of Florida — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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