Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application
Running, not enrolling
Conditions studied: Hernia, Ventral, Hernia Incisional, Hernia Incisional Ventral
In brief
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.
Key facts
- Study ID
- NCT05094089
- Run by
- W.L.Gore & Associates
- People needed
- 320
- Starts
- 2023-02-24
- Expected to finish
- 2030-07-31
- Last updated by the study team
- 2026-01-21
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Emory Saint Joseph's Hospital — Atlanta, Georgia, United States
- Tufts Medical Center — Boston, Massachusetts, United States
- Corewell Health — Grand Rapids, Michigan, United States
- Lovelace Women's Hospital — Albuquerque, New Mexico, United States
- Stony Brook University Hospital — Stony Brook, New York, United States
- Novant Health New Hanover Regional Medical Center — Wilmington, North Carolina, United States
- Prisma Health Greenville Memorial Hospital — Greenville, South Carolina, United States
- Bon Secours Memorial Regional Medical Center — Mechanicsville, Virginia, United States
- Ospedale Civile di Baggiovara — Baggiovara, Italy
- Vincenzo Monaldi Hospital — Naples, Italy
- Sapienza Università di Roma — Roma, Italy
- University Hospital Virgen Macarena - Department of General And Digestive Surgery — Seville, Spain
- Hospital Quirón Salud-Sagrado Corazón — Seville, Spain
- University Hospitals Birmingham NHS Foundation Trust - Queen Elizabeth Hospital Birmingham — Birmingham, United Kingdom
- Walsall Manor Hospital — Walsall, United Kingdom
Full record on ClinicalTrials.gov
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