Actively Recruiting
National Registry of IgG4-Related Disease in China
Led by Peking Union Medical College Hospital · Updated on 2017-01-24
900
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are establishing a nationwide registry study to gather detailed information about IgG4-related disease (IgG4-RD) patients in China. The study aims to better understand the disease's clinical features, demographics, lab and immunological characteristics, imaging, pathology, treatment, and prognosis. The study includes patients who meet the 2011 diagnostic criteria for IgG4-RD and excludes those with malignancies or other autoimmune diseases. Patients newly diagnosed with IgG4-RD will be enrolled from multiple centers across China. Data will be collected through an online system, including demographic details, symptoms, disease duration, allergy history, physical exams, organ involvement, lab results, imaging, pathology, treatments, and side effects. The study has ethical approval, and participants will provide informed consent. Participants will be followed for several years to assess organ involvement, responses to glucocorticoids and immunosuppressants, relapse rates, tumor incidence, survival rates, imaging features, and pathological diagnosis accuracy. Data analysis will be conducted using standard statistical methods, with a focus on long-term outcomes and disease behavior. The total follow-up period extends up to ten years for survival analysis.
CONDITIONS
Brief Title
National Registry of IgG4-RD in China
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis meets the 2011 comprehensive diagnostic criteria for IgG4-related disease
You will not qualify if you...
- Presence of other diseases mimicking IgG4-related disease, such as tumors, vasculitis, or sarcoidosis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 10 years
Participants who undergo routine care are observed. Data including demographic information, symptoms, disease duration, physical examinations, organ involvements, laboratory findings, imaging, pathology, treatments, and side effects are collected.
Periodic assessments over the study duration
Trial Site Locations
Total: 1 location
1
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China, 100032
Actively Recruiting
Research Team
Y
Yunyun Fei
W
Wen Zhang
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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