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RECRUITING
NCT04514965

Bezafibrate in Patients With Primary Biliary Cholangitis (PBC)

Sponsor: University of Aarhus

View on ClinicalTrials.gov

Summary

Up to 40% of patients with PBC have an inadequate response to standard treatment with UDCA, hence bezafibrate, a PPAR-agonist is being introduced as add-on therapy in these patients. sCD163, fibrosis markers and bile acid composition are of special interest in PBC. In this study, the investigators will investigate how treatment with bezafibrate influence levels of macrophage activation markers and fibrosis markers as well as bile acid composition in patients offered bezafibrate as add-on therapy to UDCA.

Official title: Measuring Macrophage Activation Markers and Influence on Bile Acid Composition in Patients With Primary Biliary Cholangitis After Treatment With Bezafibrate

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2020-10-01

Completion Date

2026-09

Last Updated

2022-08-12

Healthy Volunteers

No

Interventions

OTHER

Blood sampling

Blood sampling

DEVICE

Fibroscan

Measurement of liver stiffness

OTHER

Question

Question about pruritus

Locations (2)

Department of Hepatology and Gastroenterology, Aarhus University Hospital, Denmark

Aarhus N, Central Jutland, Denmark

Department of Medicine, Gastrounit Medical division

Hvidovre, Denmark