A COMPARISON OF TWO DOSING REGIMENS OF MISOPROSTOL IN LABOUR INDUCTION: A RANDOMIZED CONTROLLED TRIAL.
Not Applicable
- Conditions
- INDUCTION OF LABOUR IN LOW-RESOURCE SETTING
- Registration Number
- PACTR202101825071744
- Lead Sponsor
- Kwabena Amo Antwi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
Live singleton gestations at 28 weeks and above with indication for IOL.
Exclusion Criteria
Previous Caesarean section
Previous Myomectomy
Intrauterine fetal death
Multiple gestation
Breech presentation
Known allergy to misoprostol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method rate of vaginal delivery and uterine tachysystole/hyperstimulation
- Secondary Outcome Measures
Name Time Method Induction-delivery interval (IDI), need for oxytocin augmentation, passage of meconium, blood loss at vaginal delivery, 5-minute Apgar score <7, and neonatal intensive care unit (NICU) admissions were secondary outcome.