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

Study acronym: VIATIPS
StatusRecruiting
PhaseNot specified
Started
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Record History

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  1. Study sites: 2 to 3
  2. Study sites: 1 to 2
  3. Recruitment opened Show 5 more changesShow less
    • Lead sponsor: W.L.Gore & Associates to W.L.Gore & Associates
    • Study sites: 0 to 1
    • Start date changed from estimate of Jun 2026 to Jul 20, 2026
    • Eligibility criteria expanded, about 13 words
    • Secondary endpoints: details revised at 1 of 5 entries
  4. Primary endpoint revised
    • Secondary endpoints revised (5)
    v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07390344
Lead Sponsor W.L.Gore & Associates
Conditions
(from sponsor)		 Ascites, Variceal Bleeding, Portal Hypertension Related to Cirrhosis
Related terms Ascites, Fibrosis, Hypertension, Portal
Enrollment 152 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov