Clinical Trial

sCD163 in PBC Patients - Assessment of Treatment Response

Recruiting
View on ClinicalTrials.gov →
Summary
Primary biliary cholangitis (PBC) is an autoimmune chronic liver disease, characterised by destruction of the small intrahepatic bile ducts. Ursodeoxycholic acid (UDCA) is the first line treatment for patients with PBC. However, up to 40% of patients respond inadequate to this treatment. sCD163 is a macrophage activation marker shedded into plasma by macrophages in the liver. sMR is a soluble mannose receptor. The investigators want to investigate whether sCD163 and sMR can predict response to treatment with UDCA in newly diagnosed patients with PBC.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2016-10-11; most recent amendment 2022-08-11.
Trial Details
NCT Number NCT02931513
Lead Sponsor University of Aarhus
Conditions Primary Biliary Cirrhosis, Liver Inflammation, Ursodeoxycholic Acid
Enrollment 40 participants
Start Date 2016-09
Primary Completion 2031-01 (estimated)
Study Completion 2031-09 (estimated)
Updated on ClinicalTrials.gov 2022-08-12