Comparing the use of oral labour inducing agent with vaginal agent
Phase 3
Completed
- Conditions
- Health Condition 1: null- Pregnancy
- Registration Number
- CTRI/2014/02/004402
- Lead Sponsor
- Christian Medical College and Hospital Vellore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 778
Inclusion Criteria
Pregnancies between 37 to 42 weeks of gestation admitted for labor induction with live, singleton fetus
Cephalic presentation
Bishop score less than 6
Reassuring fetal heart rate
Intact membranes
Exclusion Criteria
Non-reassuring fetal heart rate
Contraindications to vaginal delivery
Previous uterine scar
Bishops score more than or equal to 7
Ruptured membranes
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method