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GORE VBX Study

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

GORE Stent
AGE: 18+ years old
GENDER: All
HEALTHY PARTICIPANTS: No
TYPE: Experimental Intervention Study
CONDITION: Symptomatic Unilateral Iliofemoral Venous Obstruction, Acute or Chronic Deep Vein Thrombosis (DVT)
COMPENSATION: No
LOCATIONS: UH Cleveland Medical Center

Learn more about this research study

Please contact the study coordinator, Janice Wolfe, at 216-844-2636 for more information or complete the online form below.

Purpose of Study

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 GORE® 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.

Request More Information

To learn more about this study, please fill out the form below to request more information.

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StudyID:

  • StudyID# 2022-01086