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Vienna Vascular Liver Disease Study (VALID)

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Medical University of Vienna

Status

Enrolling

Conditions

Porto-sinusoidal Vascular Disorder
Vascular Liver Disease
Rendu Osler Weber
Budd-Chiari Syndrome
Non-Cirrhotic Portal Hypertension
Portal Vein Thrombosis
Cardiac Cirrhosis

Study type

Observational

Funder types

Other

Identifiers

NCT03541057
VALID 1928/2017

Details and patient eligibility

About

The aim of this Register Trial is to systematically study the epidemiology, risk factors, liver function as well prognosis of patients with vascular liver diseases. Furthermore, important clinical parameters will be assessed in order to evaluate patients' coagulation status and in order to develop new biomarkers derived from blood, urine, stool or ascites of patients as well as histological samples from the upper / lower GI-tract or the liver in order to better understand the natural history of vascular liver diseases.

Full description

We will include patients with vascular liver diseases, including

  • portal vein thrombosis (PVT)
  • Budd-Chiari Syndrome (BCS)
  • Heredetary Hemorrhagic Teleangiectasia (HHT, or Osler-Rendu Disease)
  • Noncirrhotic-portal hypertension (NCPH) and Porto-sinusoidal vascular disorder
  • Cirrhosis cardiaque if the fulfill inclusion/exclusion criteria and provide written informed consent. Participation in the biobank is optional for the patients. In particular, we will study the natural course of the patients in regard to hepatic decompensation (ascites, variceal bleeding, hepatic encephalopathy), need for intensified treatment (TIPS, ICU, liver transplantation) and survival.

Enrollment

200 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of a vascular liver disease by imaging (sonography, CT, MRI), transient elastography or liver histology
  • PVT: Portal vein thrombosis
  • NCPH: non-cirrhotic Portal Hypertension
  • PSVD: porto-sinusoidal vascular disorder
  • BCS: Budd-Chiari-Syndrome
  • SOS: sinusoidal occlusive disease
  • HHT: hereditary hemorrhagic teleangiectasia
  • CIRCAD: cirrhosis cardiaque
  • Age >18 years and <100 years
  • Written informed consent obtained

Exclusion criteria

  • withdrawal of written informed consent

Trial contacts and locations

1

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Central trial contact

Bernhard Scheiner, MD; Thomas Reiberger, MD

Data sourced from clinicaltrials.gov

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