None listed
Conditions
Interventions
Intervention1: Oral Misoprostol Versus Vaginal Misoprostol: Group 1 (oral misoprostol) will receive basal unit of 20 ml (20mcg) of misoprostol solution every one hour
(prepared by dissolving one table
Sponsors
University College Of Medical Sciences
Eligibility
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of women delivering vaginally within 24 hours of induction of labour. Number of women having uterine tachysystole, non reassuring FHR, meconium stained liqour Neonatal: Apgar score (1 and 5 minute), NICU admission, Timepoint: 10 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| induction to delivery timeTimepoint: 12 hours;rate of deliveryTimepoint: 12 hours | — |
Countries
India
Contacts
Public ContactAnshika rakesh
UCMS and GTB Hospital
Outcome results
None listed