Effect of misoprostol in Cervical ripening
Not Applicable
- Conditions
- operative Hystroscopic Surgery.
- Registration Number
- IRCT201204308588N6
- Lead Sponsor
- Tehran University of Medical Sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
menopausal women and perimenopausal women without history of normal vaginal delivery;who are not pregnant at the time of examination; do not have contraindications for prostaglandins(severe asthma, glaucoma, cardiac disease, hypertension or renal failure); do not have severe uterovaginal prolapse; do not have history of cervical surgery or cervical incompetency.Exclusion criteria: history of normal vaginal delivery in perimenopausal women;pregnancy; have contraindications for prostaglandins(severe asthma, glaucoma, cardiac disease, hypertension or renal failure); have severe uterovaginal prolapse;have history of cervical surgery or cervical incompetency.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical Width. Timepoint: 10-12 hours after intervention. Method of measurement: by surgeon during operation.
- Secondary Outcome Measures
Name Time Method Time of Dilatation. Timepoint: 10-12 hours after Intervention. Method of measurement: By surgeon during operation.