Comparison of oral misoprostol with vaginal prostin for induction of labour at term with prolonged rupture of membranes

Completed

• Conditions: Pregnancy and Childbirth: Labour induction; Pregnancy and Childbirth

• Registration Number: ISRCTN57744215
• Lead Sponsor: Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-09-30
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 200

Inclusion Criteria

200 women with term rupture of membranes fitting our inclusion criteria randomised to receive prostin or misoprostol

Exclusion Criteria

Does not match inclusion criteria

Study & Design

• Study Type: Interventional
• Study Design: Not specified