Comparison of Foleys catheter along with two different routes of misoprostol for induction of labour
Not Applicable
Completed
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2021/07/035077
- Lead Sponsor
- none
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
1. Pregnant women with Single live pregnancy of more than equal to 37 weeks
2. Valid indication for induction
3. Cephalic presentation
4. Bishops score <=4
5. No foetal compromise
6. No contraindications for vaginal delivery
Exclusion Criteria
1. Cephalo pelvic disproportion on examination
2. History of antepartum haemorrhage or placenta praevia on ultrasound
3. History of previous caesarean or other uterine surgery
4. Premature rupture of membranes or Chorioamnionitis
5. Contraindications to the use of prostaglandins
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To compare the induction to delivery interval between the two groups <br/ ><br>2. To compare the number of women delivering vaginally in two groups within 24 hrs.Timepoint: induction to delivery interval
- Secondary Outcome Measures
Name Time Method 1. The maternal complications & side effects <br/ ><br>2. The fetal outcomes which includes CTG abnormalities, meconium stained liquor, <br/ ><br>APGAR score, need for neonatal resuscitation and NICU admissionTimepoint: none