GORE® ENFORM Biomaterial Product Study
Recruiting now · Not applicable
Conditions studied: Hernia, Ventral, Hernia, Hiatal, Hernia, Diaphragmatic, Incisional Hernia
In brief
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.
Key facts
- Study ID
- NCT04718168
- Run by
- W.L.Gore & Associates
- People needed
- 245
- Starts
- 2021-05-17
- Expected to finish
- 2026-09-01
- Last updated by the study team
- 2026-07-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Medical College of Wisconsin — Milwaukee, Wisconsin, United States (enrolling)
- Institute of Esophageal and Reflux Surgery — Denver, Colorado, United States (enrolling)
- University of Texas Health Science Center at Houson — Houston, Texas, United States (enrolling)
- University of California - San Diego — San Diego, California, United States (enrolling)
- Northshore University Health System Research Institute — Evanston, Illinois, United States (enrolling)
- University of Kentucky — Lexington, Kentucky, United States (enrolling)
- Prisma Health - Upstate — Greenville, South Carolina, United States (enrolling)
- Sarasota Memorial HealthCare System — Sarasota, Florida, United States
- Atrium Health — Charlotte, North Carolina, United States
Full record on ClinicalTrials.gov
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