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Clinical Trial

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

NCT: NCT07390344 · RECRUITING

NCT IDNCT07390344
StatusRECRUITING
Start Date2026-07-20
Completion2029-09-30
SponsorW.L.Gore & Associates (INDUSTRY)
First posted
Last updated

Brief 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.

Frequently Asked Questions

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

VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS) is a clinical trial registered under NCT07390344. Current status: RECRUITING.

What is the status of NCT07390344?

The current status of NCT07390344 (VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS)) is: RECRUITING.

When did VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS) start?

VIATORR® TIPS Study Evaluating 6-10mm Diameters (VIATIPS) started on 2026-07-20.

Related Devices

PMA P040027SHUNT, PORTOSYSTEMIC, ENDOPROSTHESISW. L. Gore & Associates, Inc. K152913GORE TIPS Set, GORE TIPS Sheath, GORE TIPS NeedleCreganna Medical Aslo Business AS Cregganna Tactx Medical

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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