Misoprostol In Titrated Doses to Induce Labour And Compare It With Fixed Dose Vaginal Misoprostol
Not Applicable
Completed
- Registration Number
- CTRI/2018/12/016511
- Lead Sponsor
- niversity College Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
primigravidae Women Planned for induction oflabour at 34-41 weeks period of gestation with Singleton live fetus in Cephalic presentation and Modified Bishops score �6 (unfavorable cervix) and Intact membranes and Reassuring fetal heart rate
Exclusion Criteria
Women with Prior uterine surgery (myomectomy, cornual wedge resection) or having Contraindication to misoprostol use(Previous caesarean,Renal impairment,Multiple gestation, Fetal distress or unexplained vaginal bleeding, Inflammatory bowel disease, Pre-existing heart disease, Known allergies) or Severe anemia or Fetal growth restriction or Oligohydramnios or Fetal anomaly and Unwilling to participate are excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of women delivering vaginally within 24 hours of induction of labour. <br/ ><br>Number of women having uterine tachysystole, non reassuring FHR, meconium stained liqour <br/ ><br>Neonatal: Apgar score (1 and 5 minute), NICU admission, <br/ ><br>Timepoint: 10 hours
- Secondary Outcome Measures
Name Time Method induction to delivery timeTimepoint: 12 hours;rate of deliveryTimepoint: 12 hours