🏛️ Verified NIH Record • Updated 2026-01-16
Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application (NCT05094089)
🔵 Active, Not Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: W.L.Gore & Associates
🩺 Plain-English Summary (8th-Grade Level)
The SYN 20-01 Study is a non-interventional, prospective, multicenter, multicohort, international, post-market clinical investigation looking into the assessment of GORE® SYNECOR Biomaterial in focused patient populations and in long-term application. Patients with ventral / incisional hernia amenable to hernia mesh repair will be enrolled into two cohorts (US and EU cohort) and followed-up over the period of 60 months.
Who can join: Review the eligibility criteria below.
Location: Emory Saint Joseph's Hospital — Atlanta, Georgia
Age range: 18 Years to 80 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 (15 Sites)
- Emory Saint Joseph's Hospital — Atlanta, Georgia
- Tufts Medical Center — Boston, Massachusetts
- Corewell Health — Grand Rapids, Michigan
- Lovelace Women's Hospital — Albuquerque, New Mexico
- Stony Brook University Hospital — Stony Brook, New York
- Novant Health New Hanover Regional Medical Center — Wilmington, North Carolina
- Prisma Health Greenville Memorial Hospital — Greenville, South Carolina
- Bon Secours Memorial Regional Medical Center — Mechanicsville, Virginia
- Ospedale Civile di Baggiovara — Baggiovara,
- Vincenzo Monaldi Hospital — Naples,
- Sapienza Università di Roma — Roma,
- University Hospital Virgen Macarena - Department of General And Digestive Surgery — Seville,
- Hospital Quirón Salud-Sagrado Corazón — Seville,
- University Hospitals Birmingham NHS Foundation Trust - Queen Elizabeth Hospital Birmingham — Birmingham,
- Walsall Manor Hospital — Walsall,
💰 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, Ventral
- Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation — Cleveland, Ohio
- Quadratus Lumborum Versus Placebo in Open Ventral Hernia Repair — Knoxville, Tennessee
- Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh — Mobile, Alabama
- GORE® ENFORM Biomaterial Product Study — San Diego, California
Explore by condition: All Hernia, Ventral clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.