Randomized clinical trial between two protocols of oral misoprostol for induction of labor
Phase 2
Completed
- Conditions
- abor induction.Labor induction.Reproductive Health and Childbirth - Fetal medicine and complications of pregnancy
- Registration Number
- ACTRN12613001269729
- Lead Sponsor
- Abdulrahim Rouzi.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 152
Inclusion Criteria
1.Singleton live pregnancy for induction of labor.
2.At or more than 34 weeks of gestation
3.Bishop score less than or equal to 6.
4.Intact membranes.
5.Cephalic presentation.
6.Reassuring fetal heart pattern.
Exclusion Criteria
1. Hypersensitivity to misoprostol
2. Previous C/S or other uterine surgery.
3. Severe PIH (abnormal LFT’s, protein>1g/day, BP= 160/100).
4. Para 4 and more.
5. Multiple gestation.
6. Uterine contractions.
7. Significant maternal cardiac, renal , or liver disease.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is proportion of subjects achieving vaginal delivery within 24 hours from the first dose of misoprostol.[Proportion of subjects achieving vaginal delivery before 24 hours from the first dose of misoprostol immediately after the end delivery for all participants.]
- Secondary Outcome Measures
Name Time Method