Transorb™ Self-Gripping Resorbable Mesh in High-risk Subjects Undergoing Open Repair of Ventral Hernia (NCT06449378)
Multi-center, Single-arm, Prospective Study of Transorb™ Self-Gripping REsorbable Mesh in High-risk subjeCts Undergoing Open Repair of VEntral heRnia
🩺 Plain-English Summary (8th-Grade Level)
The purpose of RECOVER is to evaluate the performance and safety of Transorb™ self-gripping resorbable mesh in high-risk subjects (at least one risk factor impairing wound healing) when used for reinforcement of abdominal wall soft tissues in procedures involving open extraperitoneal ventral hernia repair, in clean (US); and clean and clean-contaminated (Europe) surgical fields (Centers for Disease Control and Prevention (CDC) Classification I and II. Data from this study will primarily be used to support market approval and European post-market clinical follow-up needs. Secondarily, data will be used for product marketing, future product development, and to support market release and maintenance in global geographies.
Who can join: Review the eligibility criteria below.
Location: Northwestern University — Evanston, Illinois
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (13 Sites)
- Northwestern University — Evanston, Illinois
- University of Kentucky — Lexington, Kentucky
- Novant Health New Hanover Regional Medical Center — Wilmington, North Carolina
- Cleveland Clinic Foundation — Cleveland, Ohio
- The Ohio State University — Columbus, Ohio
- TPMG General Surgery and Hernia Center — Newport News, Virginia
- UZ Leuven, campus Gasthuisberg — Leuven,
- APHP Hospital Louis Mourier — Colombes,
- Centre Hospitalier Universitaire de Lille — Lille,
- Hospices Civils de Lyon — Lyon,
- Centre Hospitalier Universitaire de Reims — Reims,
- Hôpital Charles Nicolle Centre Hospitalier Universitaire de Rouen — Rouen,
- Hôpitaux Universitaires de Strasbourg — Strasbourg,
📞 Contact the Study Coordinator
Phone: (855) 692-6482
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hernia
- Image-Guided Herniorrhaphy Study — Sacramento, California
- AtraUmatic Laparoscopic HerNia Repair Clinical Investigation to Evaluate the Safety and Performance of The ECLIPSIUM System for Mesh Fixation IDE — Loma Linda, California
- Patient-reported Outcomes for Patients Undergoing Surgery at Shouldice Hospital. — Thornhill, Ontario
Explore by condition: All Hernia clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.