comparison of two different routes of T.Misoprostol 25mcg in initation of labour pain.
Not Applicable
- Conditions
- Health Condition 1: null- pregnant women
- Registration Number
- CTRI/2017/09/009632
- Lead Sponsor
- kasturba medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
Pregnant women with Singleton fetus; Cephalic presentation; Bishop Score < 6; Normal CTG
Exclusion Criteria
parity >3; Estimated fetal weight >3.5kg; Previous cesarean section; Non reassuring/abnormal fetal heart rate pattern
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method induction to delivery intervalTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method mode of the delivery, vaginal delivery within 24 hours, duration of labour, any side effects, birth weight, apgar score, neonatal intensive care unit admission.Timepoint: 24 hours