Last updated: September 27, 2022
Sponsor: Xijing Hospital of Digestive Diseases
Overall Status: Active - Recruiting
Phase
3
Condition
Hepatic Fibrosis
Liver Disorders
Primary Biliary Cholangitis
Treatment
N/AClinical Study ID
NCT02823366
KY20151230-5
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Signed informed consent
- Patient with PBC defined by 2 in 3 of the following criteria: a.Positiveantimitochondrial antibody type M2; b.Abnormal serum alkaline phosphatases (ALP > 1,5N) and aminotransferase (AST or ALT > 1N) activities; c.Histological hepaticinjuries consistent with PBC.
- Had been treated with UDCA more than 6 months, and failed to achieve a completebiochemical response.
Exclusion
Exclusion Criteria:
- Pregnancy or desire of pregnancy.
- Breast-feeding.
- Co-existing liver diseases such as acute or chronic viral hepatitis, alcoholic liverdisease, choledocholithiasis, autoimmune hepatitis, biopsy-proven non-alcoholic fattyliver disease, Wilson's disease and hemochromatosis.
- History or presence of hepatic decompensation (e.g., variceal bleeds, encephalopathy,or poorly controlled ascites).
- History of urolithiasis, nephritis or renal failure (clearance of creatinine < 60ml/mn).
- Hepatotoxic drugs use before recruiting.
- Fenofibrate anaphylaxis.
Study Design
Total Participants: 104
Study Start date:
January 01, 2016
Estimated Completion Date:
December 31, 2023
Connect with a study center
Xijing Hosipital
Xi'an, Shaanxi 710032
ChinaActive - Recruiting
Xijing Hosipital
Xi`an, Shaanxi 710032
ChinaSite Not Available

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