Overview
Oral Misoprostol Solution in Labor Induction
Status:
Unknown status
Unknown status
Trial end date:
2020-01-18
2020-01-18
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
This study compares safety and efficacy between repetitive hourly dose of oral misoprostol and two hourly dose oral regimens for cervical ripening and labor induction.Phase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Ain Shams UniversityTreatments:
Misoprostol
Criteria
Inclusion Criteria:- Nulliparas
- Term pregnancy(equal or more than 37 wks)
- Bishop score <6
- Cephalic presentation
- reassuring fetal heart rate pattern
- Not in labor ( no uterine contractions)
- Clinically adequate pelvis
- Singleton live pregnancy
Exclusion Criteria:
- Allergic to misoprostol or prostaglandin analogues
- Previous uterine scar( cesarean section,hysterotomy,myomectomy)
- Multiple fetal gestations
- Fetal demise
- Preterm labor
- Malpresentations
- Non reactive cardiotocography at admission
- Cephalo pelvic disproportion
- Fetal macrosomia