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Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application — SYN 20-01  

Hernia, Ventral Clinical Trial

Official title:
Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05094089
Study type Observational
Source W.L.Gore & Associates
Contact Heidie Hornstra O'Neill
Phone +14439073152
Email hhornstr@wlgore.com
Status Recruiting
Phase
Start date February 24, 2023
Completion date December 31, 2028
View Details
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