Pre-induction ripening of the cervix using foleys catheter alone and combination of foleys and prostaglandin gel
Not Applicable
Completed
- Conditions
- Health Condition 1: null- pregnancy needing induction of labour
- Registration Number
- CTRI/2017/12/010737
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 110
Inclusion Criteria
1. pregnant women undergoing labour induction
2. gestation 34 weeks or more
3. single live fetus, cephalic,
4.intact membranes,
5. Bishop score 6 or less
Exclusion Criteria
1. medical disorders,
2. parity 4 or more,
3. uterine scar,
4. severe IUGR,
5. severe PE/E, 6.
fetal anomaly,
7. APH
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method induction delivery intervalTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Caesarean rate <br/ ><br>maternal and neonatal outcome <br/ ><br>Timepoint: 24 hours <br/ ><br>3days