Key Insights

Highlights

Success Rate

90% trial completion (above average)

Published Results

21 trials with published results (18%)

Research Maturity

72 completed trials (62% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

6.9%

8 terminated out of 116 trials

Success Rate

90.0%

+3.5% vs benchmark

Late-Stage Pipeline

15%

17 trials in Phase 3/4

Results Transparency

29%

21 of 72 completed with results

Key Signals

21 with results90% success

Data Visualizations

Phase Distribution

74Total
Not Applicable (46)
Early P 1 (1)
P 1 (2)
P 2 (8)
P 3 (5)
P 4 (12)

Trial Status

Completed72
Unknown20
Terminated8
Recruiting6
Not Yet Recruiting4
Active Not Recruiting3

Trial Success Rate

90.0%

Benchmark: 86.5%

Based on 72 completed trials

Clinical Trials (116)

Showing 20 of 20 trials
NCT07360691Not ApplicableCompletedPrimary

Prospective Clinical Evaluation of High-Purity Type I Collagen in Select High-Risk Hernia Repair Scenarios

NCT07166172Not ApplicableRecruiting

Prospective Registry for Long-term Outcomes Following FETO in Severe Left and Right CDH

NCT07267494Not ApplicableNot Yet RecruitingPrimary

Image-Guided Herniorrhaphy Study

NCT07419958Not ApplicableCompleted

Effects of Relaxation Exercises on Fear of Movement, Pain, and Quality of Life in Lumbar Disc Herniation Patients

NCT07401446Not ApplicableCompletedPrimary

Complication Rate of Onlay vs Sublay Mesh Repair in Incisional Hernia

NCT06485440Completed

The Effects of Preoperative Botulinum Toxin A Injection on Respiratory System Function

NCT07316426Not ApplicableRecruitingPrimary

Preoptimisation in Ventral Hernia Surgery

NCT02527083Phase 4Completed

Influence of Anesthetic Technique on Acute and Chronic Neuropathic Pain

NCT07277946Not ApplicableNot Yet RecruitingPrimary

AtraUmatic Laparoscopic HerNia Repair Clinical Investigation to Evaluate the Safety and Performance of The ECLIPSIUM System for Mesh Fixation IDE

NCT07220382Phase 4Recruiting

Preoperative BOTOX® Injection for Large Ventral Hernia Repair

NCT01727388Phase 3Completed

Informativeness to Digital Rectal Examination

NCT07157501Not ApplicableCompleted

Aromatherapy Versus Acupressure: Impact on Postoperative Pain and Sleep Quality in Pediatric Abdominal Surgery Patients

NCT06449378Not ApplicableActive Not RecruitingPrimary

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

NCT06042205Not ApplicableActive Not RecruitingPrimary

TISSIUM™ Atraumatic Hernia Repair System (TAHRS) Pilot Study

NCT06034652CompletedPrimary

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

NCT02439060Not ApplicableCompleted

PUBMIC (Prophylactic Use of Biologic Mesh in Ileal Conduit)

NCT02781870Not ApplicableRecruitingPrimary

Laparoscopic Groin Hernia Repair by a 3D ENDOLAP Visible Mesh With or Without LiquiBand Fix 8 Mesh Fixation

NCT06789744Not ApplicableNot Yet Recruiting

Enhanced Recovery After Urologic Surgery

NCT05142618Not ApplicableActive Not Recruiting

Pilot Trial of Abdominal Core Rehabilitation To Improve Outcomes After Ventral Hernia Repair

NCT06717061Enrolling By InvitationPrimary

Composed Abdominal Wall Analysis. Collecting Tissue and Blood From Patients Undergoing Elective Laparosopic Cholecystectomy. Objective to Describe the Normal Abdominal Wall

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