Key Insights

Highlights

Success Rate

97% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

2.0%

1 terminated out of 51 trials

Success Rate

96.6%

+10.0% vs benchmark

Late-Stage Pipeline

12%

6 trials in Phase 3/4

Results Transparency

25%

7 of 28 completed with results

Key Signals

7 with results97% success

Data Visualizations

Phase Distribution

37Total
Not Applicable (30)
P 2 (1)
P 3 (1)
P 4 (5)

Trial Status

Completed28
Unknown8
Recruiting5
Withdrawn4
Active Not Recruiting3
Not Yet Recruiting2

Trial Success Rate

96.6%

Benchmark: 86.5%

Based on 28 completed trials

Clinical Trials (51)

Showing 20 of 20 trials
NCT04779918Not ApplicableRecruitingPrimary

Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh

NCT03201744Not ApplicableWithdrawnPrimary

Prospective Randomized Trial of Moderate vs Deep Neuromuscular Blockade During Laparoscopic Ventral Hernia Repair

NCT06879912Recruiting

A Study to Understand the Utility of the Force Feedback Instruments in Robotic Procedures Using da Vinci 5 Robot

NCT07422441Not ApplicableNot Yet RecruitingPrimary

Compliance-Guided Abdominal Wall Closure Strategy in Large Ventral Hernia Repair

NCT04718168Not ApplicableRecruitingPrimary

GORE® ENFORM Biomaterial Product Study

NCT05094089Active Not RecruitingPrimary

Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

NCT07316426Not ApplicableRecruiting

Preoptimisation in Ventral Hernia Surgery

NCT06051578Active Not RecruitingPrimary

Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation

NCT05985343Phase 4CompletedPrimary

The Impact of Sugammadex on Ileus After Abdominal Wall Reconstruction

NCT06449378Not ApplicableActive Not Recruiting

Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia

NCT02228889Not ApplicableCompletedPrimary

RCT of Two Noncrosslinked Porcine Acellular Dermal Matrices in Ab Wall Reconstruction

NCT06034652Completed

T-GENVIH-003 LTFU (Long Term Follow Up) Study

NCT06953635Not ApplicableNot Yet RecruitingPrimary

Quadratus Lumborum Versus Placebo in Open Ventral Hernia Repair

NCT05734222Not ApplicableRecruitingPrimary

Optimization of Surgical Treatment of Patients With Incisional Ventral Hernias

NCT06409091CompletedPrimary

Short Term Outcomes of Heavy-weight Versus Medium-weight Synthetic Mesh

NCT05446675CompletedPrimary

Endoscopic eTEP Versus Open Rives-Stoppa

NCT05320055CompletedPrimary

Pain and Readmission After Lap IPOM vs. Robotic Ventral Hernia Repair

NCT04355819Not ApplicableCompletedPrimary

Patient Centered Outcomes Study

NCT05912868CompletedPrimary

Endoscopic Mini/Less Open Sublay(EMILOS) Repair

NCT03074474Not ApplicableCompletedPrimary

Ventral Hernia Study Using OviTex Reinforced Bioscaffold

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Research Network

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