Comparison of the effect of letrozole /Estradiol and Misoprostol in labor inductio
Phase 2
- Conditions
- labor.Death from direct obstetric cause
- Registration Number
- IRCT2014120920264N1
- Lead Sponsor
- Vice chancellor for research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Gestational age over 36 weeks; singleton pregnancy with a vertex presentation; the absence of contraindications to vaginal delivery
Exclusion criteria: Indication for emergency childbirth; History of liver and kidney disease; History of fetal distributors; History of contraindications use misoprostol (such as the mother's risk of blood coagulation disorders, asthma, glaucoma, etc).
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cervical ripening. Timepoint: The Bishop score less than 4 until the Bishop score of above 7. Method of measurement: vaginal exam.
- Secondary Outcome Measures
Name Time Method Duration of delivery. Timepoint: Every 4 hours. Method of measurement: vaginal exam.