Condition
Provoked Localized Vulvodynia
Total Trials
5
Recruiting
1
Active
1
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
33%
1 of 3 completed with results
Key Signals
1 with results100% success
Data Visualizations
Phase Distribution
4Total
Not Applicable (3)
P 1 (1)
Trial Status
Completed3
Enrolling By Invitation1
Recruiting1
Trial Success Rate
100.0%
Benchmark: 86.5%
Based on 3 completed trials
Clinical Trials (5)
Showing 5 of 5 trials
NCT06999395Not ApplicableRecruiting
Does a Virtual Program for Pelvic Pain Improve Pain and Sexual Outcomes in Individuals With Provoked Vestibulodynia?
NCT03541512Not ApplicableEnrolling By InvitationPrimary
Remote Mindfulness Education PLV
NCT02919813Not ApplicableCompletedPrimary
M-gCBT for Women With Provoked Localized Vulvodynia
NCT02712814CompletedPrimary
Subtypes of Provoked Vestibulodynia
NCT01996384Phase 1CompletedPrimary
Provoked, Localized Vulvodynia Treatment With Acupuncture and Lidocaine Pilot Study
Showing all 5 trials