Efficacy of Prostaglandine E2 and intra-cervical Foley balloon in labor inductio
Phase 2
Completed
- Conditions
- induction of labor.Single spontaneous delivery
- Registration Number
- IRCT201012071760N10
- Lead Sponsor
- Vice Chancellor for Research and Technology, Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 89
Inclusion Criteria
Term pregnant women (37-42 weeks), first pregnancy that had indication of labor and Bishop Score less than 5. Exclusion criteria: Rupture of membrane, Twin pregnancy, Preterm labor and closed cervix.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preinduction cervical ripening. Timepoint: 12 to 48 hours after intervention. Method of measurement: Clinical examinations.
- Secondary Outcome Measures
Name Time Method se of induction. Timepoint: 12 to 48 hours after entries. Method of measurement: Clinical examinations.;Type of delivery. Timepoint: 12 to 48 hours after entries. Method of measurement: Clinical examinations.;Infant status. Timepoint: 12 to 48 hours after entries. Method of measurement: Clinical examinations.;Possible complication. Timepoint: 12 to 48 hours after entries. Method of measurement: Clinical examinations.