VICIS - Vienna Cirrhosis Study

NCT03267615 · tracked via the Priya Life Science Austria tracker

Sponsor

Medical University of Vienna

Phase

Observational

Started

2017-02-01

Last updated

2025-09-25

Condition(s) studied

Liver CirrhosisPortal HypertensionAscitesVariceal HemorrhageHepatic Encephalopathy

Study summary

Patients with advanced chronic liver diseases treated at the Vienna General Hospital of the Medical University of Vienna will be offered to participate in this prospective observational trial - including an optional participation in a biobank.

Clinical parameters and laboratory parameters will be recorded for all patients and patients will undergo a regular follow-up schedule with clinical visits at the Vienna General Hospital.

This study is linked to a biobank with serum/plasma, ascitic fluid, urine, GI tract mucosal biopsies, liver biopsies and stool collected from the study participants.

Eligibility

Sex

ALL

Min age

18 Years

Max age

100 Years

Healthy volunteers

Inclusion Criteria: * Age \>18 years and \<100 years * Diagnosis of advanced chronic liver disease (by liver stiffness ≥10kPa, HVPG\>5mmHg or Histology F3/F4) * Written informed consent Exclusion Criteria: * Withdrawal of written informed consent

Primary outcome measure(s)

Transplant-free survival — 01/FEB/2017 - 31/DECEMBER/2027
Time from inclusion to death or liver transplantation

Trial sites (1)

Facility	City	Region	Status
Medical University of Vienna	Vienna	Austria	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03267615 on ClinicalTrials.gov ↗ ← All trials in Austria