Unfavorable Cervix
6
1
1
2
Key Insights
Highlights
Success Rate
100% trial completion (above average)
Clinical Risk Assessment
Based on trial outcomes
Low Risk
Score: 27/100
0.0%
0 terminated out of 6 trials
100.0%
+13.5% vs benchmark
17%
1 trials in Phase 3/4
50%
1 of 2 completed with results
Key Signals
Data Visualizations
Phase Distribution
Trial Status
Trial Success Rate
Benchmark: 86.5%
Based on 2 completed trials
Clinical Trials (6)
Oxytocin vs Prostaglandins for Labor Induction of Women With an Unfavorable Cervix After 24h of Cervical Ripening
Heated Saline in Cervical Balloon for Labor Induction, a RCT
Randomized Control Trial of Intracervical Balloon Placement vs Oxytocin in Women With Term PROM and Unripe Cervices
Balloon Catheter Combined With Oxytocin Induction Among the Pregnant Women With Previous Cesarean Section
Cervical Ripening in Premature Rupture of Membranes
Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours