Last updated: August 28, 2023
Sponsor: Wuhan Union Hospital, China
Overall Status: Active - Recruiting
Phase
N/A
Condition
Primary Biliary Cholangitis
Treatment
Collect stool and blood samples from patients
Clinical Study ID
NCT05448144
UHCT22032
Ages 18-70 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- The group of ALD:
- aged >18 years;
- patients who meet the diagnostic criteria of ALD in Chinese Guideline for thePrevention and Management of Alcoholic Liver Disease (2018 Update);
- history of chronic heavy alcohol consumption;
- with relatively complete clinical data and good compliance.
- The group of purely drinking:
- aged >18 years;
- history of chronic alcohol consumption;
- no evidence of fatty liver, hepatitis or liver injury.
- The group of healthy control:
- aged >18 years;
- without history of alcohol consumption;
- no evidence of fatty liver, hepatitis or liver injury.
Exclusion
Exclusion Criteria:
- with hepatocellular carcinoma or hepatic metastases;
- combined with infectious liver diseases, such as hepatitis A virus, hepatitis B virus,hepatitis C virus, hepatitis D virus, hepatitis E virus and human immunodeficiencyvirus (HIV);
- combined with non-infectious liver diseases, such as non-alcoholic fatty liverdisease, drug-induced hepatitis, autoimmune liver disease, Immunoglobulin G subclass 4-related liver disease, Wilson's disease, alpha 1-antitrypsin deficiency, Budd-Chiarisyndrome, and other congenital liver diseases;
- combined with severe organic lesions of other organs;
- pregnant and lactating women.
Study Design
Total Participants: 200
Treatment Group(s): 1
Primary Treatment: Collect stool and blood samples from patients
Phase:
Study Start date:
June 01, 2022
Estimated Completion Date:
December 31, 2024
Study Description
Connect with a study center
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei 430022
ChinaActive - Recruiting
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