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.
Hernia, Ventral, Hernia Incisional, Hernia Incisional Ventral
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.
Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application
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Emory Saint Joseph's Hospital, Atlanta, Georgia, United States, 30342
Tufts Medical Center, Boston, Massachusetts, United States, 02111
Corewell Health, Grand Rapids, Michigan, United States, 49506
Lovelace Women's Hospital, Albuquerque, New Mexico, United States, 87109
Stony Brook University Hospital, Stony Brook, New York, United States, 11794
Novant Health New Hanover Regional Medical Center, Wilmington, North Carolina, United States, 28401
Prisma Health Greenville Memorial Hospital, Greenville, South Carolina, United States, 29605
Bon Secours Memorial Regional Medical Center, Mechanicsville, Virginia, United States, 23116
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
For general information about clinical research, read Learn About Studies.
18 Years to 80 Years
ALL
No
W.L.Gore & Associates,
2028-12-31