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ANA Pattern Recognition System and Research on ANA New Target Antigen

Antinuclear Antibody Pattern Recognition System and Research on ANA New Target Antigen

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074070
Enrollment
Unknown
Registered
2023-07-28
Start date
2024-01-01
Completion date
Unknown
Last updated
2023-07-30

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

Conditions

autoimmun disease

Interventions

autoimmune disease group:NA
healthy control group:NA

Sponsors

Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: From January to June 2024, the clinical residual serum of patients with autoantibody detection in Renji Hospital, and meet any of the following requirements: a. Anti-nuclear antibody indirect immunofluorescence detection is one of the 30 ANA patterns defined by ICAP, with a single karyotype and a titer >1:320; b. Clinically diagnosed as autoimmune disease, antinuclear antibody indirect immunofluorescence titer > 1:320, and common ANA autoantibodies results are negative; c. Clinically diagnosed systemic lupus erythematosus, Sjogren's syndrome, systemic sclerosis, mixed connective tissue disease, immune myopathy, autoimmune liver disease, and undifferentiated connective tissue disease.

Exclusion criteria

Exclusion criteria: a. The sample information is confusing and vague; b. Sample volume less than 0.5mL c. Severe jaundice, severe lipemia, severe hemolysis, severe pollution

Design outcomes

Primary

MeasureTime frame
antinuclear antibody;

Countries

China

Contacts

Public ContactBing Zheng

Renji Hospital, School of Medicine, Shanghai Jiao Tong University

85750524@qq.com+86 133 9148 8484

Outcome results

None listed

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