Vienna Vascular Liver Disease Study

NCT ID: NCT03541057

Last Updated: 2024-01-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-12-12

Study Completion Date

2024-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medical University of Vienna

OTHER

Sponsor Role lead

Responsible Party

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Thomas Reiberger

Assoc.-Prof. Priv.-Doz. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medical University of Vienna

Vienna, , Austria

Site Status RECRUITING

Countries

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Austria

Central Contacts

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Thomas Reiberger, MD

Role: CONTACT

0043140400 ext. 47410

Bernhard Scheiner, MD

Role: CONTACT

0043140400 ext. 47410

Facility Contacts

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Thomas Reiberger, MD

Role: primary

0043140400 ext. 47410

Bernhard Scheiner, MD

Role: backup

0043140400 ext. 47410

Other Identifiers

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VALID 1928/2017

Identifier Type: -

Identifier Source: org_study_id

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