Last reviewed · How we verify

VIATORR Device Registry

NCT05661331 ACTIVE_NOT_RECRUITING

The primary objective is to confirm the clinical performance and safety of the GORE® VIATORR® TIPS (Transjugular Intrahepatic Portosystemic Shunt) Endoprosthesis with Controlled Expansion throughout the device functional lifetime of 3 years in real world setting. The secondary objective is to collect information on quality of life after treatment with the GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion. Additionally, data will be collected on the safety and performance of the GORE TIPS Set when utilized.

Details

Lead sponsorW.L.Gore & Associates
StatusACTIVE_NOT_RECRUITING
Enrolment196
Start dateTue Feb 21 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionSun Dec 31 2028 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

France, Italy, Austria, Germany, Spain