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Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation

Premature Birth Clinical Trial

Official title:
Randomized Trial Comparing Misoprostol and Foley Bulb for Labor Induction in the Preterm Gestation

Clinical Trial Summary

The purpose of this study is to compare the time to delivery of two different cervical ripening methods on the preterm gestation.

Clinical Trial Description

Labor induction for the preterm gestation is indicated for various maternal and fetal indications. The preterm cervix, however, is frequently not favorable for induction. Multiple methods have been evaluated in the term gestation. As these comparison studies have not included the preterm gestation, this study seeks to evaluate these two methods in terms of safety, efficacy and time to delivery. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00325026
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase Phase 2
Start date April 2005
Completion date April 2007
View Details
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