Randomized trial comparing efficacy of 12.5 and 25 µg oral misoprostol 2 hourly for induction of labor
Phase 3
- Conditions
- Induction of labor in maternal and fetal conditionInduction of labor ,misoprostol ,success rate
- Registration Number
- TCTR20191230002
- Lead Sponsor
- donthani hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Enrolling by invitation
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
women with singleton live pregnancy , Gestational age greater than or equal to 38 weeks , have indication of induction of labor , vertex presentation, normal fetal heart rate , Bishop score less than or equal to 6 point , intact membrane
Exclusion Criteria
refuse participate in research , misoprostol allergy , previous cesarean section or myomectomy ,underlying disease such as heart, renal ,liver disease ,severe preeclampsia with severe feature , Grand multiparity ,regular uterine contraction , multifetal pregnancy , active genital tract disease , DFIU and fetal anomaly , estimate fetal weight more than 4000 grams
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of successful induction of labor within 24 hours , comparing 12.5 and 25 µg oral misoprostol Induction time to delivery time successful induction of labor was defined as vaginal delivery within 24 hr can be achieved
- Secondary Outcome Measures
Name Time Method maternal and neonatal outcome after delivery period analyzed data of maternal and neonatal outcome after delivery,rate of uterine tachysystole , rate of cesarean section after delivery period record data and analyzed data after delivery