Condition
Delivery Uterine
Total Trials
5
Recruiting
0
Active
0
Completed
3
Success Rate
100.0%+13% vs avg
Key Insights
Highlights
Success Rate
100% trial completion (above average)
Clinical Risk Assessment
Based on trial outcomes
Moderate Risk
Score: 50/100
Termination Rate
0.0%
0 terminated out of 5 trials
Success Rate
100.0%
+13.5% vs benchmark
Late-Stage Pipeline
0%
0 trials in Phase 3/4
Results Transparency
0%
0 of 3 completed with results
Key Signals
100% success
Data Visualizations
Phase Distribution
5Total
Not Applicable (4)
P 2 (1)
Trial Status
Completed3
Unknown2
Trial Success Rate
100.0%
Benchmark: 86.5%
Based on 3 completed trials
Clinical Trials (5)
Showing 5 of 5 trials
NCT02570620Not ApplicableCompletedPrimary
Contribution of Ultrasonography in the Evaluation of Cervical Induction-delivery Time
NCT02655783Not ApplicableCompletedPrimary
Use of Normal Saline With or Without Dextrose During Induction of Labor in Nulliparous
NCT01765881Phase 2CompletedPrimary
Comparison Between 25 µg Vaginal Misoprostol vs Slow Release Pessary PGE2
NCT01506102Not ApplicableUnknownPrimary
Thromboelastography During and After Delivery
NCT01505192Not ApplicableUnknownPrimary
Noninvasive Continuous Measurement of SpHb After Spontaneous Vaginal Delivery
Showing all 5 trials