Clinical Trial

VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS)

Study acronym: VIATIPS
Not Yet Recruiting
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Summary
This Registry will look at patients being treated with a transjugular intrahepatic portosystemic shunt (TIPS) procedure for portal hypertension. The purpose of this Registry is to collect data on the safety and performance of the GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion (6-10mm) for 2 years in real world setting. Additionally, data will be collected on the safety and performance of the GORE TIPS Set when utilized.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-28.
Trial Details
NCT Number NCT07390344
Lead Sponsor W.L.Gore & Associates
Conditions Ascites, Variceal Bleeding, Portal Hypertension Related to Cirrhosis
Enrollment 152 participants
Start Date 2026-06
Primary Completion 2029-09-30 (estimated)
Study Completion 2029-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-02-10