Condition: Aortic Arch Dissection · Aortic Arch Aneurysm · Sponsor: W.L.Gore & Associates
A prospective multi-center post-market study collecting outcomes through at least 5-years and up to 10-years post procedure for subjects treated with the TBE Device in Zone 0/1 as part of routine clinical practice.
This description comes directly from the study's public registry record.
DeAnne Hart · 800-437-8181 · tbe25-03@wlgore.com
Always discuss trial participation with your own doctor first.
| Keck Medical Center of USC | Los Angeles, California, United States | Recruiting |
| Hartford Hospital | Hartford, Connecticut, United States | Recruiting |
| University of Florida Health Heart & Vascular | Gainesville, Florida, United States | Recruiting |
| Lakeland Regional Medical Center | Lakeland, Florida, United States | Recruiting |
| University of South Florida | Tampa, Florida, United States | Recruiting |
| Duke University Medical Center | Durham, North Carolina, United States | Recruiting |
| The Methodist Hospital-Houston | Houston, Texas, United States | Recruiting |
| Baylor Scott & White Research Institute | Plano, Texas, United States | Recruiting |
| Intermountain Medical Center | Murray, Utah, United States | Recruiting |
| University of Washington Medical Center | Seattle, Washington, United States | Recruiting |
| University of Wisconsin - Madison | Madison, Wisconsin, United States | Recruiting |
| Medical College of Wisconsin | Milwaukee, Wisconsin, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07166133