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Recruiting NCT02931513

NCT02931513 sCD163 in PBC Patients - Assessment of Treatment Response

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Clinical Trial Summary
NCT ID NCT02931513
Status Recruiting
Phase
Sponsor University of Aarhus
Condition Primary Biliary Cirrhosis
Study Type OBSERVATIONAL
Enrollment 40 participants
Start Date 2016-09
Primary Completion 2031-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Blood samplesFibroscanQuestionnaires

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 40 participants in total. It began in 2016-09 with a primary completion date of 2031-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * Newly diagnosed with Primary biliary cholangitis * No treatment with UDCA Exclusion Criteria: * Patient under 18 years * Expected lifetime under 6 months * Expected liver transplantation within 6 months * Liver cancer * Cirrhosis from other causes

Contact & Investigator

Central Contact

Lars Bossen, PhD-student

✉ larsbossen@clin.au.dk

📞 +4522800676

Frequently Asked Questions

Who can join the NCT02931513 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Primary Biliary Cirrhosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02931513 currently recruiting?

Yes, NCT02931513 is actively recruiting participants. Contact the research team at larsbossen@clin.au.dk for enrollment information.

Where is the NCT02931513 trial being conducted?

This trial is being conducted at Aarhus C, Denmark.

Who is sponsoring the NCT02931513 clinical trial?

NCT02931513 is sponsored by University of Aarhus. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology