Comparison between misoprostol and oxytocine in cervical ripening for labour induction: a randomized clinical trial
Phase 2
Completed
- Conditions
- Failed medical induction of labour.Failed induction (of labour) by:•oxytocin•prostaglandins
- Registration Number
- IRCT2012103011324N1
- Lead Sponsor
- Ahwaz Jundishapur University of Medical Science, Vice Chancellor for Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 190
Inclusion Criteria
Entry criteria : Medical indication for the induction of delivery; Single twin pregnancies; Gestational age more than 36 weeks; Vertex presentation ;The normal heart rate of embryos .The exit criteria: The embryo-pelvic dystocia; An estimated weight of over 4000 grams or evidence of a lack of fitness cephalopelvic ; Abnormal vaginal bleeding or any placenta previa; The number of pregnancy over 4; Fetal malformation; Previous uterine scar; Any situation that does not cause vaginal delivery indication, Any contraindication use of misopristol ; Severe polyhydramnios
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bishop index. Timepoint: Baseline and every 30 minutes during the intervention and at the end of the intervention. Method of measurement: The questionnaire.
- Secondary Outcome Measures
Name Time Method Infantile complication. Timepoint: Baseline and every 30 minutes during the intervention and at the end of the intervention. Method of measurement: Apgar score.