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

Full record on ClinicalTrials.gov

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