Comparison of two methods of delivery in women with severe pre eclampsia at term
Phase 4
- Conditions
- Health Condition 1: O141- Severe pre-eclampsia
- Registration Number
- CTRI/2021/04/032534
- Lead Sponsor
- Principal Midnapore Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Diagnosis of severe pre-eclampsia in singleton pregnancy at equal or more than 37 weeks of gestation
Exclusion Criteria
1.Diagnosis of hypertension of systolic blood pressure < 160 mm of Hg and diastolic blood pressure <110 mm Hg with medication
2.Women in labour ( cervical dilatation < 4 cm )
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure will be a composite endpoint of maternal mortality, maternal complications (eclampsia, HELLP syndrome, pulmonary oedema, thromboembolic disease) <br/ ><br>Primary neonatal outcome will be Apgar score of 3 or below, admission to the neonatal intensive care unit (NICU) or neonatal death <br/ ><br>Timepoint: at baseline
- Secondary Outcome Measures
Name Time Method 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