GORE® ENFORM Biomaterial Product Study (NCT04718168)
GORE® ENFORM Biomaterial Product Study: A Study to Describe Multi-use Biomaterial Performance in Hernia Patients
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of California - San Diego — San Diego, California
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (9 Sites)
- University of California - San Diego — San Diego, California
- Institute of Esophageal and Reflux Surgery — Denver, Colorado
- Sarasota Memorial HealthCare System — Sarasota, Florida
- Northshore University Health System Research Institute — Evanston, Illinois
- University of Kentucky — Lexington, Kentucky
- Atrium Health — Charlotte, North Carolina
- Prisma Health - Upstate — Greenville, South Carolina
- University of Texas Health Science Center at Houson — Houston, Texas
- Medical College of Wisconsin — Milwaukee, Wisconsin
📞 Contact the Study Coordinator
Phone: (443) 907-3152
Email: hhornstr@wlgore.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hernia, Ventral
- Abdominal Wall Tension in Patients Undergoing Ventral Hernia Repair Without Component Separation — Cleveland, Ohio
- Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application — Atlanta, Georgia
- Quadratus Lumborum Versus Placebo in Open Ventral Hernia Repair — Knoxville, Tennessee
- Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh — Mobile, Alabama
Explore by condition: All Hernia, Ventral clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.