Actively Recruiting

All Genders
ID03023371

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis meets the 2011 comprehensive diagnostic criteria for IgG4-related disease
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

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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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