Clinical Trial: Viatorr CX Case-control Study for Complications of Portal Hypertension

Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Observational




Official Title: Viatorr Control Expansion Compared to Bare-metal and Regular Viatorr for Complications of Portal Hypertension

Brief Summary: To evaluate the clinical benefits in the patients receiving Viatorr CX over a period of 12 months of structured Follow-up (before TIPS, at TIPS, 1 week after TIPS, at 6 weeks, 4 months, 6 months, 9 months, 12 months), regarding clinical endpoints, such as HE, readmission, liver injury, cardiac function, response to TIPS and the passive expansion of the stents in real life.