Ventral Hernia Clinical Trial
Official title:
A Prospective Study of Fortiva in Hernia Repair
The goal of this study is to evaluate safety and performance of the Fortiva Tissue Matrix. Participants will complete questionnaires to measure outcomes after hernia surgery for two years.
This is a post market, prospective, multi-center study of up to 120 participants at approximately 10 clinical study sites. Safety and performance will be measured after hernia repair for two years. ;
Status | Clinical Trial | Phase | |
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Recruiting |
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N/A | |
Recruiting |
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Completed |
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N/A | |
Completed |
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N/A | |
Not yet recruiting |
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Completed |
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Evaluation of Ultrasound-guided Erector Spinae Block for Postoperative Analgesia in Laprascopic Ventral Hernia Repair.
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N/A | |
Recruiting |
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Video-based Collaborative Learning to Improve Ventral Hernia Repair
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Recruiting |
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Phase 2/Phase 3 | |
Completed |
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Randomized Control Trial Comparing Transfascial Suture for Mesh Fixation to No Mesh Fixation
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N/A | |
Completed |
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The Influence of Closing the Gap on Postoperative Seroma and Recurrences in Laparoscopic Ventral Hernia Repair
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N/A | |
Completed |
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Transverse Abdominis Plane Block in Laparoscopic Ventral Hernia Repair
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N/A | |
Completed |
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Comparing eTEP and Laparoscopic Intraperitoneal Onlay Mesh (IPOM) for Ventral Hernias
|
N/A | |
Recruiting |
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Ventral Hernia Prevention After Liver Transplantation
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N/A | |
Completed |
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Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair
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Terminated |
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The Use of Biologic Mesh vs Bioabsorbable Mesh During Ventral Hernia Repair in At-risk Patients
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N/A | |
Completed |
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A Clinical Trial Using Spy Elite System in Planning Tissue Advancement Flaps After Ventral Hernia Repair
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N/A |