Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Conditions
Interventions
Control Intervention1: Not Applicable: Not Applicable
Control Intervention2: Oral Misoprostol: B. Oral misoprostol 25 mcg taken orally repeated every 2 hours up to a maximum of 5 doses
Control Interve
Sponsors
Dept Of Obstetrics And Gynecology
Eligibility
Inclusion criteria
Inclusion criteria: • Singleton with Cephalic presentation • Nulliparous and multiparous women who had completed 36 weeks of gestation • Modified Bishop’s score • Normal fetal heart tracing available prior to induction
Exclusion criteria
Exclusion criteria: 1. Documented Cephalopelvic disproportion 2. Prior caesarean delivery/ previous scarring on the uterus 3. Signs of labour (regular painful contractions with cervical change) 4. Fetal demise or known major fetal anomaly 5. Antepartum haemorrhage 6. Cerclage in the current pregnancy 7. Oligohydramnios, defined as amniotic fluid index 8. Fetal growth restriction, defined as EFW 9. Chronic medical disorders i.e., chronic hypertension, pregestational diabetes mellitus, renal diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the proportions of caesarean deliveries with the use of misoprostol through three methodsTimepoint: After delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| i. Time from induction to vaginal delivery, ii. Incidence of Pathological CTG iii. Indications for cesarean delivery, iv. Uterine hyperstimulation v. Maternal Post-partum hemorrhage, vi. Puerperal Pyrexia vii. Number of sterile vaginal examinations performed viii. Duration and dose of oxytocin augmentation required ix. Change in neonatal cord blood gases at birth x. Unplanned admission to the NICU Timepoint: before and after delivery | — |
Countries
India
Contacts
Public ContactDr Anu Anna George
MOSC MEDICAL COLLEGE HOSPITAL
Outcome results
None listed