Study Results
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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RECRUITING
200 participants
OBSERVATIONAL
2017-12-12
2024-12-31
Brief Summary
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Detailed Description
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* 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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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* 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
18 Years
100 Years
ALL
No
Sponsors
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Medical University of Vienna
OTHER
Responsible Party
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Thomas Reiberger
Assoc.-Prof. Priv.-Doz. Dr.
Locations
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Medical University of Vienna
Vienna, , Austria
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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VALID 1928/2017
Identifier Type: -
Identifier Source: org_study_id
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