Comparision of different methods to initiate cervical changes before labour.
Phase 3
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/04/066341
- Lead Sponsor
- Kshirabdhi Tanaya Mohapatra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Singleton pregnancy
2)Term gestation (37-42 weeks)
3)Cephalic presentation
4)Reactive admission NST
5)Bishop score less than or equal to 6
6)Intact Membranes
Exclusion Criteria
1)Previous Lower Segment Cesarean Section
2)Contra-indications of prostaglandins and Vaginal delivery
3)Malpresentation
4)Already diagnosed Mullerian anomalies
5)Hypersensitivity to Prostaglandins and Mifepristone
7)Active Vaginal infections.
8)Placental abnormalities (low lying Placenta)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the efficacy of synthetic osmotic cervical dilator (DILAPAN-S) vs Dinoprostone vaginal gel for cervical ripening in induction of labourTimepoint: Baseline (48-72 hours)
- Secondary Outcome Measures
Name Time Method To determine fetomaternal outcomeTimepoint: Baseline (48-72 hours)