The GORE® VIAFORT Vascular Stent Iliofemoral Study
- Study HIC#:2000035340
- Last Updated:05/12/2025
This study is a prospective, non-randomized, multicenter, single-arm, clinical study to evaluate the performance, safety and efficacy of the GORE® VIAFORT Vascular Stent for treatment of symptomatic iliofemoral venous obstruction.
- Age18 years and older
- GenderBoth
Contact Us
For more information about this study, including how to volunteer, contact:
Cassius Iyad Ochoa Chaar
- Phone Number: 1-203-737-2481
Help Us Discover!
You can help our team find trials you might be eligible for by creating a volunteer profile in MyChart. To get started, create a volunteer profile, or contact helpusdiscover@yale.edu, or call +18779788343 for more information.
Eligibility Criteria
One of the following:
- Clinical severity class of CEAP ‘C’ classification ≥3 or rVCSS pain score ≥2.
- Patient has adequate inflow to the target lesion(s), per investigator/sub-investigator discretion, involving at least a patent femoral or deep femoral vein.
- Presence of non-malignant symptomatic unilateral iliofemoral venous obstruction.
