Condition: Hernia, Ventral · Hernia, Hiatal · Hernia, Diaphragmatic · Sponsor: W.L.Gore & Associates
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.
This description comes directly from the study's public registry record.
Shelli Ryczek · 928 864 3640 · ENF1806@wlgore.com
Always discuss trial participation with your own doctor first.
| University of California - San Diego | San Diego, California, United States | Recruiting |
| Institute of Esophageal and Reflux Surgery | Denver, Colorado, United States | Recruiting |
| Sarasota Memorial HealthCare System | Sarasota, Florida, United States | Recruiting |
| Northshore University Health System Research Institute | Evanston, Illinois, United States | Recruiting |
| University of Kentucky | Lexington, Kentucky, United States | Recruiting |
| Atrium Health | Charlotte, North Carolina, United States | Recruiting |
| Prisma Health - Upstate | Greenville, South Carolina, United States | Recruiting |
| University of Texas Health Science Center at Houson | Houston, Texas, United States | Recruiting |
| Medical College of Wisconsin | Milwaukee, Wisconsin, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04718168