Oral misoprostol compared to intracervical Foley catheter for induction of labour
Phase 3
Completed
- Conditions
- Induction of labour
- Registration Number
- SLCTR/2016/024
- Lead Sponsor
- Department of Obstetrics and Gynecology Faculty of Medicine, University of Ruhuna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
1. Women with uncomplicated pregnancies
2. 40 weeks + 5 days gestation
3. Modified Bishop score (MBS) of < 6
4. Singleton pregnancy
5. Cephalic presentation
6. Intact membranes
Exclusion Criteria
1. Pregnancy induced hypertension
2. Gestational diabetes mellitus
3. Fetal growth restriction
4. Previous caesarean delivery
5. Scarred uterus
6. Hypersensitivity to misoprostol
7. Contraindication for a vaginal delivery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method