Comparison of characteristics of women undergoing labor induction with oxytocin and oral misoprostol
Phase 2
- Conditions
- Induction of Labor.Failed medical induction of labour
- Registration Number
- IRCT2012080610511N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 65
Inclusion Criteria
39 to 42 weeks of gestational age; Estimated fetal weight 4000 g; Normal fetal heart rate; cephalic presentation; Absence of uterine contractions; Singleton pregnancy; Bishop score of 7 or less. Exclusion criteria: Previous uterine surgery including caesarean section; Intrauterine fetal death IUGR; Oligohidroamnius; Placenta previa; Umbilical cord Prolapse; Corioamnionitis symptoms; Symptoms of active herpes; kidney or liver disease; NST Non-Stress Test reactive bread; Contraindication for Administration of prostaglandin. Contraindication for induction of labor; Vaginal bleeding of unknown cause.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of induction to active phase. Timepoint: During 12, 18, 24 hours. Method of measurement: clock.;Start time of induction to delivery. Timepoint: During 12, 18, 24 hours. Method of measurement: clock.
- Secondary Outcome Measures
Name Time Method