Comparison of the effect of misoprostol with oxytocin in companion with a cervical catheter in the induction of labor: a clinical trial
Phase 3
Recruiting
- Conditions
- labor induction.
- Registration Number
- IRCT20101227005485N8
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 50
Inclusion Criteria
Pregnancy age of 37 weeks and over
indication for termination of pregnancy
primiparous women
singleton pregnancy
reassuring fetal heart rate
cephalic presentation
intact fetal membranes
ineffective labor contractions
Bishop Score 6 or below
Exclusion Criteria
Misoprostol allergy
fever over 38 °C
history of uterine surgery and cesarean
obstetric indication for cesarean delivery
anemia and blood dyscrasia
asthma
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The time to ripen the cervix. Timepoint: every two hours. Method of measurement: vaginal examination.;Duration of latent phase of labor. Timepoint: every two hours. Method of measurement: vaginal examination.
- Secondary Outcome Measures
Name Time Method Duration of active phase of labor. Timepoint: every hour. Method of measurement: vaginal examination.;Duration of second stage of labor. Timepoint: every half hour. Method of measurement: vaginal examination.;Complication rate. Timepoint: Continuous during labor. Method of measurement: fetal monitoring.