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Clinical Characteristics and Treatment Outcomes in Primary Biliary Cholangitis Patients with Elevated Immunoglobulin G Levels

Clinical Characteristics and Treatment Outcomes in Primary Biliary Cholangitis Patients with Elevated Immunoglobulin G Levels

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122826
Enrollment
Unknown
Registered
2026-04-19
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary biliary cholangitis

Interventions

The IgG elevated PBC group and the IgG normal PBC group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years; 2. Meet the diagnostic criteria for primary biliary cholangitis; 3. Alanine aminotransferase and aspartate aminotransferase levels below 5 times the upper limit of normal; 4. Received standard-dose ursodeoxycholic acid therapy for at least 1 year, with or without concomitant immunosuppressive therapy; 5. Follow-up duration at the study center of at least 1 year.

Exclusion criteria

Exclusion criteria: 1. Coexisting other autoimmune liver diseases, including primary sclerosing cholangitis, autoimmune hepatitis, or any type of overlap syndrome; 2. Coexisting viral hepatitis, alcoholic liver disease, fatty liver disease, drug-induced liver injury, or hereditary liver disease; 3. Missing key baseline or follow-up data; 4. Ursodeoxycholic acid therapy duration of less than 1 year or suboptimal dosage; 5. Follow-up duration of less than 1 year.

Design outcomes

Primary

MeasureTime frame
Biochemical remission;Death;Liver transplantation;Relapse;

Secondary

MeasureTime frame
Time to obtain complete remission;

Countries

China

Contacts

Public ContactYang Li

West China Hospital, Sichuan University

yangli_hx@scu.edu.cn+86 189 8060 1276

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026