A randomised controlled trial comparing combined misoprostol-foley's catheter with foley's catheter and low dose misoprostol for cervical ripening.
Not Applicable
- Conditions
- Pregnancy and ChildbirthInduction of labour
- Registration Number
- PACTR201312000680425
- Lead Sponsor
- Ekiti State University Teaching Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 210
Inclusion Criteria
Singleton pregnancies for induction of labour for various obstetrics reasons.
Exclusion Criteria
1.Previous caesarean section patients
2.Previous history of anaphylactic reaction to misoprostol
3.History of asthmatic attack
4.History of prelabour rupture of membrane
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time interval it takes for ripening of the cervix to be acheived
- Secondary Outcome Measures
Name Time Method abour and Neonatal outcomes/complications