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A clinical study of biliary atresia treatment with Belimumab

Immune pathogenesis and treatment of biliary atresia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046985
Enrollment
Unknown
Registered
2021-06-06
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-18

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

Conditions

biliary atresia

Interventions

Control Group:Conventional therapy
Experimental group:Belimumab

Sponsors

Guangzhou Women and Children Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.1 Years to 0.3 Years

Inclusion criteria

Inclusion criteria: 1. The subjects of this study were recruited from the Hepatobiliary Surgery Department of Guangzhou Women and Children's Medical Center who were diagnosed with highly suspected BA by experienced doctors, and the patients were planned to undergo hepatobiliary surgery; 2. 0-3 months old children with obstructive jaundice; 3. A clear diagnosis of BA by intraoperative cholangiography; 4. Normal hematopoietic function; 5. The guardian's informed consent.

Exclusion criteria

Exclusion criteria: 1. Children with systemic inflammatory response syndrome or multiple system malformations; 2. Children with unclear diagnosis of the primary disease.

Design outcomes

Primary

MeasureTime frame
Liver function indexes;Lymphocytes count;Detection of autoantibody;BAFF concentration;

Countries

China

Contacts

Public ContactWen Zhe

Guangzhou Women and Children Medical Center

wenzhe2005@163.com+86 18902268782

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026