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GORE VBX Study

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Evaluation of the GORE® VIAFORT Vascular Stent for Treatment of Symptomatic Iliofemoral Venous Obstruction

  • Sex: Any
  • Age: Adult (18 - 64), Older Adult (65+)
  • Accepting Healthy People: No
  • Type: Interventional / Device
  • Trial Phase: NA
  • Conditions Being Studied: Iliofemoral Venous Obstruction

Study Purpose

The purpose of this research study is to look at treating reduced blood flow through the veins in one of your legs (common iliac, external iliac, and/or common femoral veins), known as iliofemoral venous disease, with an investigational study device called the GOREĀ® VIAFORT Vascular Stent, and to evaluate the safety and efficacy of the study device.

Who Can Participate

Participants 18 years and older who have been diagnosed with symptomatic unilateral iliofemoral venous obstruction, with acute or chronic DVT, may be eligible for this study.

Principal Investigator
Karem Harth MD
Department/Division
Heart and Vascular (Vascular)

Locations

UH Cleveland Medical Center
11100 Euclid Ave
Cleveland OH, 44106

  • UH IRB: SITE00001878
  • StudyID: 2022-01086
  • ClinicalTrials.gov: NCT05489588
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