This is a study to compare the outcome of inducing laborby using a tube inserted in cervix along with misoprostol medication either as oral solution oras tablet kept under your tongue among women in their first pregnancy at term gestation requiring induction of labor
Phase 2
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Nulliparous women = 18 years of age
2)Gestational age = 37 weeks
3)Singleton pregnancy, vertex presentation
4)Bishop’s score less than or equal to 4
Exclusion Criteria
1)Women with severe pre-eclampsia
2)Premature rupture of membranes
3)Previously scarred uterus (myomectomy/ septal resection)
4)Previous anaphylaxis to prostaglandins
5)Abnormal FHR changes
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Proportion of successful vaginal deliveryTimepoint: 72 hours after insertion of foleys catheter
- Secondary Outcome Measures
Name Time Method Maternal & fetal outcomeTimepoint: 72 hours after insertion of foleys catheter;Time from induction to deliveryTimepoint: 72 hours after insertion of foleys catheter