Efficiency of mifepristone to facilitate vaginal delivery
Phase 4
- Conditions
- Health Condition 1: null- Pregnant patients after 40 weeks, to assess the effect of drug on labour
- Registration Number
- CTRI/2018/05/013743
- Lead Sponsor
- Government Medical College Kozhikode
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Singleton pregnancy, cephalic presentation
Gestational age after 40 weeks
No cephalopelvic disproportion
Normal latest USG
Reactive NST
Intact membranes
Bishop score <6
Without any medical complications
Exclusion Criteria
Myoma/Uterine surgery
Parity more than 3
Severe hypertension or preeclampsia
Prior cesarean deliveries
Diabetes
Impaired renal,adrenal or hepatic function
Fetal malformation
Breech presentation
Cephalopelvic disproportion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome <br/ ><br>1. Improvement in Bishop,s score <br/ ><br>2. Time interval between induction and delivery <br/ ><br>3. Requirement of induction <br/ ><br>4. Requirement of augmentation <br/ ><br>5. Cesarean rate <br/ ><br>6. Failure of induction <br/ ><br> <br/ ><br>Timepoint: till delivery
- Secondary Outcome Measures
Name Time Method Any maternal or fetal side effectsTimepoint: till patient is discharged from the hospital