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 15 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

7%

1 trials in Phase 3/4

Results Transparency

13%

1 of 8 completed with results

Key Signals

1 with results100% success

Data Visualizations

Phase Distribution

10Total
Not Applicable (8)
P 2 (1)
P 4 (1)

Trial Status

Completed8
Recruiting3
Active Not Recruiting3
Unknown1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 8 completed trials

Clinical Trials (15)

Showing 15 of 15 trials
NCT04880239Not ApplicableActive Not RecruitingPrimary

REDUCE Trial- Reducing Prolapse Recurrence

NCT06159777Phase 4Completed

Pre-operative Polyethylene Glycol 3350 for Minimally Invasive Urogynecologic Surgery

NCT07194343Not ApplicableCompleted

Posterior Mesh Fixation at the Levator Ani Level in Apical Pelvic Organ Prolapse

NCT05760794Not ApplicableActive Not RecruitingPrimary

Barbed-suture Efficiency Study for Sacrocolpopexy

NCT05836844RecruitingPrimary

Pragmatic Evaluation of Performance and Safety of the Anchorsure® Transvaginal Device for Surgical Treatment of Apical Prolapse in Women

NCT05978414Not ApplicableRecruitingPrimary

Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

NCT04491617Not ApplicableCompleted

STandard Versus No Opioid Prescription After Prolapse and Anti-INcontinence Surgery Trial

NCT06404931Phase 2RecruitingPrimary

Transvaginal Human Acellular Dermal Matrix for Prolapse Treatment

NCT05633901Not ApplicableActive Not Recruiting

Impact of Preop Video on Patient Anxiety

NCT06128291CompletedPrimary

Concomitant Posterior Colporrhaphy on Bowel Functions in Pelvic Organ Prolapse Repair

NCT06620211CompletedPrimary

Evaluation of the Safety, Performance, and Tolerability of the Sacromesh® Medical Device in the Treatment of Prolapse by Promontofixation in a Population of Patients Followed Over the Long Term.

NCT04440475Not ApplicableCompleted

Tap Block vs Conventional Pain Medication for Patients Undergoing Robotic Sacrocolpopexy

NCT06352112Not ApplicableCompleted

Effects of the Hypopressive Exercises in Women With Pelvic Organ Prolapse

NCT05750615UnknownPrimary

What Affects Willingness to Self-manage a Pessary?

NCT03878056CompletedPrimary

Cost-effectiveness Comparison Between Vaginal Versus Robotic Mesh Surgery for Apical Prolapse: Prospective, Cohort Study

Showing all 15 trials

Research Network

Activity Timeline