Effectiveness of vaginal isosorbide mononitrate for cervical ripening in uncomplicated singleton pregnancies at 39 weeks gestation in an outpatient setting: A randomized controlled trial
Early Phase 1
Completed
- Conditions
- Induction of labour
- Registration Number
- SLCTR/2013/030
- Lead Sponsor
- niversity of Ruhuna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
1.Uncomplicated pregnancy at 39 weeks POG
2.Singleton fetus having a cephalic presentation
3. Modified Bishop's Score <5
4.Consenting to self-administer the vaginal tablets every other day for five doses.
Exclusion Criteria
1.Any pregnancy complications e.g. Pregnancy Induced Hypertension, Gestational Diabetes Melitus
2.Multiple pregnancies
3.Planned Caesarean section
4.Fetal Growth Restriction
5.History of hypersensitivity or idiosyncratic reaction to nitrates.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method