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Clinical Trial Summary

Several risk assessment scoring systems have been proposed to assess the therapeutic response and predict long term prognosis in ursodeoxycholic acid (UDCA)-treated primary biliary cholangitis (PBC) patients, in order to risk stratify PBC patients and guide their management. However there scoring systems have not been fully validated in Chinese population. This study is going to compare the prognostic ability of these criteria, validate the overseas scoring systems, develop and validate a new scoring system in a cohort of Chinese PBC patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03188146
Study type Observational
Source Humanity and Health Research Centre
Contact George Lau, MD, PhD
Phone 28613777
Email gkklau@hnhmgl.com
Status Recruiting
Phase
Start date May 1, 2017
Completion date May 1, 2028

See also
  Status Clinical Trial Phase
Not yet recruiting NCT03521297 - Probiotics in PBC Patients of Poor Response to UDCA Phase 2
Recruiting NCT05896124 - CS0159 in Chinese Patients With PBC (Primary Biliary Cholangitis) Phase 2
Recruiting NCT06016842 - A Long-Term Study of Elafibranor in Adult Participants With Primary Biliary Cholangitis Phase 3
Completed NCT04047160 - Safety, Tolerability of OP-724 in Patients With Primary Biliary Cholangitis (Phase I) Phase 1
Completed NCT03124108 - Study to Evaluate the Efficacy and Safety of Elafibranor in Patients With Primary Biliary Cholangitis (PBC) and Inadequate Response to Ursodeoxycholic Acid Phase 2