The Comparison of Vaginal Misoprostol with buccal and sublingual Misoprostol in Labor Induction in Term Pregnancy
Phase 2
Recruiting
- Conditions
- induction of labour.
- Registration Number
- IRCT20180121038465N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 300
Inclusion Criteria
single, bishop score=4, cephalic presentation, NST reactive, parity =2, gestational age more than 37 w, Amniotic fluid index =5
Exclusion Criteria
maternal medical diseases
breech presentation
fetal anomaly
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The effect of misoprostol in induction of labor. Timepoint: every 6h to 24h. Method of measurement: bishop score and time of delivery.
- Secondary Outcome Measures
Name Time Method The rate of Cesarean section. Timepoint: delivery. Method of measurement: cesarean/ NVD.;Reason of cesarean. Timepoint: during delivery. Method of measurement: mecunium, FHR deceleration, No responce to induction.;Time to the active phase of labor. Timepoint: 0-6-24 hr. Method of measurement: Bishop Score.;Need for oxytocin. Timepoint: until delivery. Method of measurement: yes/no.;Number of misoprostol doses. Timepoint: until delivery. Method of measurement: 1-2-3.;Fetal complications. Timepoint: until delivery. Method of measurement: abnormal pattern of fetal heart rate, meconium, Apgar score 1 and 5 postpartum, and admission to neonatal intensive care unit.;Maternal complication. Timepoint: until delivery. Method of measurement: Fever, chills, nausea, vomiting, uterine tachysystole, uterine hyperstimulation.