To compare the safety and efficacy of 'low dose' vaginal misoprostol and dinoprostone vaginal gel for induction of labour at term

Completed

• Conditions: Pregnancy and Childbirth: Induction of labour; Pregnancy and Childbirth

• Registration Number: ISRCTN85744560
• Lead Sponsor: Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2003-09-12
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

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

Inclusion Criteria

1. Women at term (37-42 completed weeks of pregnancy)
2. Single fetus, cephalic presentation
3. Membranes may be intact or ruptured
4. Reactive fetal heart tracing

Exclusion Criteria

Does not match inclusion criteria

Study & Design

• Study Type: Interventional
• Study Design: Not specified