GORE VBX Study
Evaluation of the GORE® VIAFORT Vascular Stent for Treatment of Symptomatic Iliofemoral Venous Obstruction
GENDER: All
HEALTHY PARTICIPANTS: No
CONDITION: Symptomatic Unilateral Iliofemoral Venous Obstruction, Acute or Chronic Deep Vein Thrombosis (DVT)
COMPENSATION: No
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.
StudyID:
- StudyID# 2022-01086