A comparison of the efficacy of concurrent use of intracervical foley catheter balloon and mifepristone to intracervical foley catheter alone for cervical ripening at term: a triple-blind randomized control trial
- Conditions
- Pregnancy and Childbirth
- Registration Number
- PACTR202306488956692
- Lead Sponsor
- ESE ADIGBA ONODJOHWOYOVWE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 112
All Consented pregnant women with the following:
1.Term pregnancy
2. Singleton foetus in cephalic presentation
3.Intact foetal membrane
4.Normal non stress test
5.Bishop Score of < 6
6.No contraindication to vaginal delivery
7.No known allergy or contraindication to Mifepristone.
1. Preterm pregnancy
2. Prolonged pregnancy (=42 weeks gestation)
3. Prelabour rupture of foetal membrane
4. Previous caesarean section or major uterine surgery
5. Bishop score = 6 at admission
6. Foetal malpresentation
7. Multiple pregnancy
8. Intrauterine foetal death,
9. Severe intrauterine growth restriction
10. Severe oligohydramnios
11. Major congenital anomalies
12. Allergy or contraindication to use of Mifepristone
13. Abnormal or non-reassuring non stress test
14. Contraindication to vaginal delivery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method