Status: Recruiting
GORE® ENFORM Biomaterial Product Study
A prospective, retrospective, non-randomized, multicenter study with two independent hernia study cohorts (Ventral / Incisional Hernia Repair and Diaphragmatic / Hiatal Hernia Repair). The primary objective of this study is to collect GORE® ENFORM Biomaterial product commercial-use data on device functional performance and short-term patient experience.
Participants needed: 245
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: W.L.Gore & AssociatesUpdated: Feb 18, 2026Locations: 9
Eligibility criteria
At least 18 years old at the time of informed consent. Minimum age required by s... [+4]
Treated in another drug or medical device study within 1 year of study enrollmen... [+28]