A comparative analytical study of initiation of labour in a term live pregnancy with oral mifepristone tablet v/s intracervical dinoprostone gel in their safety, efficacy and fetomaternal outcome.
Not Applicable
- Conditions
- Health Condition 1: null- Pregnant woman at term with indication for induction of labour.
- Registration Number
- CTRI/2017/08/009325
- Lead Sponsor
- IPGMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Postmaturity ( >40-41weeks)
2) Premature rupture of membranes.
3) Oligohydramnios.
4) Congenital malformation of the fetus.
5) Various maternal conditions( Such as- chronic hypertension and diabetes etc).
6) Bishopâ??s score <6 at time of inclusion .
Exclusion Criteria
1) Major Cephalopelvic disproportion.
2) Multifetal pregnancy.
3) Malpresentation.
4) Previously scarred uterus.
6)Woman who does not give informed written consent.
7) Mothers age below 18 years.
8.)Unexplained vaginal bleeding, placenta previa .
9) Medical problemâ??s like impaired renal/hepatic or adrenal function.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Vaginal delivery achieved within 48 hoursTimepoint: 48 hours
- Secondary Outcome Measures
Name Time Method 1. Induction to delivery interval. <br/ ><br>2. Bishopâ??s score improvement after 24 hours. <br/ ><br>3. Requirement for augmentation. <br/ ><br> 4. Requirement of instrument assisted delivery or caesarean delivery. <br/ ><br> <br/ ><br>5. Incidence of serious neonatal morbidity or perinatal mortality. <br/ ><br>6. Incidence of serious maternal morbidity / mortality <br/ ><br> <br/ ><br>Timepoint: 48 hours