Comparing the use of oral misoprostol with vaginal misoprostol to facilitate spontaneous labour
Phase 3
- Registration Number
- CTRI/2019/01/017318
- Lead Sponsor
- Fluid Research Grant
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Singleton pregnancy between 39-40 weeks
Cephalic presentation with live fetus
Bishop score <6 at 39weeks
Lack of current indication for Induction of labour
Gestational Diabetes on Medical Nutrition Therapy
Exclusion Criteria
Ruptured membranes
Unexplained vaginal bleeding
Prior uterine incision
Gestational Hypertension
Gestational Diabetes on Oral Hypoglycemic Agents & Insulin
Estimated fetal weight >= 4000gm
Bad obstetric history
Pregnancy by Assisted reproductive technology
Malpresentations
Multiple gestation
Uterine anomaly
Bishop score >= 6
Poor dates
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method