NCT00886860

The Comparison of Efficacy for Cervical Ripening in Labor Induction Between Titrated and Conventional Oral Misoprostol

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 64 (actual)
• Sponsor: Mahidol University · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: Accepted

Summary

The purpose of this study is to compare the efficacy for cervical ripening in labor induction between titrated and conventional oral misoprostol

Conditions

• Cervical Ripening
• Labor Induction

Interventions

Type	Name	Description
DRUG	misoprostol	misoprostol 50 micrograms oral every 4 hours until cervical dilatation 3 cm
DRUG	misoprostol	misoprostol 20 micrograms oral every hours until cervical dilatation 3 cm

Timeline

• Start date: 2009-05-01
• Primary completion: 2009-12-01
• Completion: 2010-03-01
• First posted: 2009-04-23
• Last updated: 2010-07-14

Locations

1 site across 1 country: Thailand