vaginal misoprostol versus laminaria for cervical ripeing in full term pregnants. A comparative randomized trial
Not Applicable
- Conditions
- vaginal delivery.Spontaneous vertex delivery
- Registration Number
- IRCT2013010712037N1
- Lead Sponsor
- Kashan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Inclusion criterion: single pregnants with unriped cervix.
Exclusion criteria: noncephalic presentation; sever preeclampsia; intrauterine growth restriction(IUGR); presence of uterine contractions; fetal distress; oligohydramnios and rupture of fetal membranes.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Dilatation of cervix. Timepoint: On admission, 6 hours later and then every 2 hours. Method of measurement: Vaginal exam based on Bishop Score.;Induction to delivery time. Timepoint: Since induction of labor to delivery. Method of measurement: Calculating time(hour).
- Secondary Outcome Measures
Name Time Method Fetal distress. Timepoint: Every 15 minutes. Method of measurement: Auscultation of fetal heart.;Thick meconium. Timepoint: Time of membrane rupture. Method of measurement: Vaginal examination.