Health Condition 1: O141- Severe pre-eclampsia
Conditions
Interventions
Intervention1: Induction of labour versus Cesarean Delivery: Women will be randomly allocated to either caesarean delivery (experimental arm) or induction of labour (control arm). The study will be an
Sponsors
Principal Midnapore Medical College
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosis of severe pre-eclampsia in singleton pregnancy at equal or more than 37 weeks of gestation
Exclusion criteria
Exclusion criteria: 1. Diagnosis of hypertension of systolic blood pressure 2. Women in labour ( cervical dilatation 3. Multiple pregnancy , Intrauterine fetal death 4. Any contraindication to vaginal delivery or induction of labour such as Cephalopelvic dis proportion , malpresentation, post cesarean pregnancy ,placenta previa Fetal macrosomia , Fetal distress , IUGR
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure will be a composite endpoint of maternal mortality, maternal complications (eclampsia, HELLP syndrome, pulmonary oedema, thromboembolic disease) Primary neonatal outcome will be Apgar score of 3 or below, admission to the neonatal intensive care unit (NICU) or neonatal death Timepoint: at baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary neonatal outcomes will be newborn sepsis, confirmed seizures, necrotizing enterocolitis, hypoxic-ischemic encephalopathy, cardiopulmonary resuscitation or ventilator support within 24 hours after birth,Timepoint: At baseline | — |
Countries
India
Contacts
Public ContactBheshna Sahu
Midnapore Medical college
Outcome results
None listed