Premaquick Pre-induction Cervical Assessmen Trial
Not Applicable
- Conditions
- Pregnancy and Childbirth
- Registration Number
- PACTR201604001592143
- Lead Sponsor
- DR GEORGE ELEJE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 170
Inclusion Criteria
Pregnant women scheduled for induction of labor at or beyond 37 weeks of gestation
Singleton pregnancy
Cephalic presentation
Intact membranes
Unfavourable cervix (Bishop score <6)
Exclusion Criteria
Non-vertex presentation
Uterine scars other than one prior low transverse cesarean section
Multiple gestation
Premature rupture of membranes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method percentage of women with unripe cervix, i.e. the percentage of women who will be administered prostaglandin (misoprostol) as a preinduction agent;interval from start of induction to any type of delivery;Uterine rupture
- Secondary Outcome Measures
Name Time Method eed for oxytocin augmentation;Interval from start of induction to beginning of active phase;Number of women with spontaneous rupture of membranes and interval from start of induction to this event;Route of delivery;Number of women with cesarean section for failed induction;Meconium passage;Birth weight;Apgar scores;Number of infants admitted to neonatal intensive care unit