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Characterisation of Patients With Primary Biliary Cholangitis in Austria - A Prospective Registry and Biobank

Status: Recruiting
Location: See all (11) locations...
Study Type: Observational
SUMMARY

The goal of this registry is to better understand how primary biliary cholangitis develops over time, including the role of disease-related biomarkers, complications of the disease, and symptom burden. Patients with primary biliary cholangitis treated at participating centres in Austria will be invited to take part in this prospective registry. Participation in an associated biobank is optional. Clinical and laboratory data will be collected, and patients will be followed regularly through scheduled clinic visits. In addition, biological samples (serum, plasma, and, if available, liver tissue) may be collected and stored in the biobank for future research.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age \>18 years

• Confirmed diagnosis of primary biliary cholangitis (at least two of the following three criteria must be fulfilled: persistent elevation of alkaline phosphatase above the upper limit of normal for at least 6 months; presence of antimitochondrial antibodies or PBC-specific antinuclear antibodies; characteristic histopathology)

• Written informed consent for participation in the registry

Locations
Other Locations
Austria
Medizinische Universität Graz
NOT_YET_RECRUITING
Graz
Medizinische Universität Innsbruck
NOT_YET_RECRUITING
Innsbruck
Klinikum Klagenfurt am Wörthersee
NOT_YET_RECRUITING
Klagenfurt
Kepler Universitätsklinikum
NOT_YET_RECRUITING
Linz
Ordensklinikum Linz - Barmherzige Schwestern
NOT_YET_RECRUITING
Linz
Universitätsklinikum Salzburg
NOT_YET_RECRUITING
Salzburg
Universitätsklinikum St. Pölten
NOT_YET_RECRUITING
Sankt Pölten
Klinik Landstraße
NOT_YET_RECRUITING
Vienna
Klinik Ottakring
NOT_YET_RECRUITING
Vienna
Medizinische Universität Wien
RECRUITING
Vienna
Klinikum Wels-Grieskirchen
NOT_YET_RECRUITING
Wels
Contact Information
Primary
Michael Trauner, MD
Michael.Trauner@meduniwien.ac.at
+43 1 40400 47410
Backup
Benedikt S Hofer, MD
Benedikt.S.Hofer@meduniwien.ac.at
+43 1 40400 47410
Time Frame
Start Date: 2026-03-18
Estimated Completion Date: 2040-12
Participants
Target number of participants: 500
Sponsors
Collaborators: Medical University Innsbruck, Klinik Ottakring, Salzburger Universitätsklinkum, Klinikum Wels-Grieskirchen, Universitätsklinikum St. Pölten, Klinikum Klagenfurt am Wörthersee, Kepler University Hospital, Medical University of Graz, Krankenanstalt Rudolfstiftung, Ordensklinikum Linz GmbH Krankenhaus Barmherzige Schwestern
Leads: Medical University of Vienna

This content was sourced from clinicaltrials.gov