The GORE® VIABAHN® FORTEGRA Venous Stent IVC Study
Running, not enrolling · Not applicable
Conditions studied: Venous Thromboses, Venous Disease, Venous Leg Ulcer, Venous Stasis, Venous Ulcer, Venous Stenosis, Venous Occlusion, Vein Thrombosis, Vein Occlusion, Vein Disease
In brief
This study is a prospective, multicenter, non-randomized, single-arm study to evaluate the performance, safety, and efficacy of the GORE® VIABAHN® FORTEGRA Venous Stent (formerly known as GORE® VIAFORT Vascular Stent) for treatment of symptomatic inferior vena cava obstruction with or without combined iliofemoral obstruction in adult patients.
Key facts
- Study ID
- NCT05409976
- Run by
- W.L.Gore & Associates
- People needed
- 136
- Starts
- 2022-10-25
- Expected to finish
- 2030-05-09
- Last updated by the study team
- 2026-04-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Stanford University School of Medicine — Stanford, California, United States
- MedStar Washington Hospital Center — Washington D.C., District of Columbia, United States
- Northwestern — Chicago, Illinois, United States
- University of Michigan — Ann Arbor, Michigan, United States
- Mount Sinai Medical Center — New York, New York, United States
- Weill Cornell Medical College — New York, New York, United States
- Atrium Health-Sanger Heart and Vascular Institute — Charlotte, North Carolina, United States
- Sentara — Norfolk, Virginia, United States
- Flinders Medical Centre — Adelaide, South Australia, Australia
- Universitätsklinikum Aachen — Aachen, Germany
- Alexianer Klinikum Hochsauerland GmbH — Arnsberg, Germany
- University College Hospital GALWAY /Clinical Research Facility Galway — Galway, Connacht, Ireland
- Ospedale San Raffaele — Milan, Italy
- Hesperia Hospital — Modena, Italy
- Auckland City Hospital — Auckland, New Zealand
- Addenbrooke's Hospital — Cambridge, United Kingdom
- St Thomas' Hospital — London, United Kingdom
Full record on ClinicalTrials.gov
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