Effectiveness and safety of oral misoprostol Vs intravaginal PGE2 (Dinoprostone) for pre-induction cervical ripening in women with uncomplicated, singleton, post dated pregnancies: a randomized controlled study.
Phase 4
Completed
- Conditions
- Induction of labour
- Registration Number
- SLCTR/2021/022
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
•Nulliparous pregnant women
•In a singleton pregnancy
•At 40 weeks and 5 days of gestation
•Fetus in cephalic presentation with intact membranes
•Modified bishop score(MBS) of < 5
•Not having any contraindications for vaginal delivery
Exclusion Criteria
•past caesarian delivery
•history of myomectomy
•hypersensitivity to misoprostol
•pregnancy induced hypertension
•gestational diabetes mellitus
•multiple pregnancies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method