National Registry of IRPF in China

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04314323
Collaborator
(none)
500
1
119.5
4.2

Study Details

Study Description

Brief Summary

The aim of this study is to establish a nation-wide cohort study of idiopathic retroperitoneal fibrosis (IRPF) in China.

Methods: All the patients fulfilling diagnostic criteria of IRPF would be enrolled from multi-centers around China. A online database system has been established.

Endpoints: The primary endpoint is to investigate the clinical manifestations of Chinese IRPF patients; the secondary endpoints including the demographic features,laboratory characteristics, immunological tests, imaging and pathological features, in addition, the treatment and prognosis of the disease.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a multicenter registry study of IRPF patients. Newly diagnosed IRPF patients will be recruited from all over the China. Inclusion criteria: patients with newly diagnosed IRPF will be recruited. Exclusion criteria: patients with secondary forms of retroperitoneal fibrosis or malignancy are excluded.

    The data will be uploaded through the platform of Chinese Rheumatology Information Platform. Demographic data, initial symptoms, disease duration, history of allergy, and physical examination, organ involvements, laboratory findings, radiological and pathological results, as well as treatment, side effects will be recorded.

    This study was approved by the Medical Ethics Committee of PUMCH (Beijing, China). All patients will sign informed consent.

    Statistical Analysis: All parameters are described in the standard summary statistics, including mean, standard deviation, minimum, and maximum. All statistical analyses will be performed by SPSS.

    Endpoints: The primary endpoint is to investigate the organ involvements of Chinese IRPF patients. The secondary endpoints include the demographic features,laboratory characteristics, immunological tests, imaging and pathological features, in addition, the treatment and prognosis of the disease.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    National Registry of Idiopathic Retroperitoneal Fibrosis in China
    Anticipated Study Start Date :
    Mar 17, 2020
    Anticipated Primary Completion Date :
    Mar 1, 2030
    Anticipated Study Completion Date :
    Mar 1, 2030

    Outcome Measures

    Primary Outcome Measures

    1. Organ involvements of Chinese IRPF patients [5 years]

      To calculate the percentage of organ involvements in at least 500 patients.

    Secondary Outcome Measures

    1. Response rate of treatment with glucocorticoids and immunosuppressants on IRPF in China [5 years]

    2. Relapse rate of IRPF patients in China [5 years]

    3. The correlation between baseline disease activities and relapse rate. [5 years]

    4. Ten year survival rate of patients with IRPF in China. [10 years]

    5. The imaging features of involved organs. [3 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Conforming to the diagnostic criteria of IRPF;Definite IRPF must have the following characteristics: (1) The typical finding of Imaging shows retroperitoneal mass, surrounding the abdominal aorta and iliac arteries, with encasement of ureters and/or organ dysfunction; (2) Exclusion of disease progression after standard glucocorticoid treatment; and (3) histopathological findings shows a fibrous tissue with signs of chronic inflammation. The inflammatory component is comprised of lymphocytes, plasma cells and macrophages. Neutrophils and granulomas are rare findings. Possible IRPF required (1) and (2), but without histopathological examination.
    Exclusion Criteria:
    • None of them met the criteria for other autoimmune diseases. None had malignant disease. Secondary forms of RPF related to drugs, infections, malignancies, Erdheim-Chester disease and IgG4-RD, need to be excluded.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Peking Union Medical College Hospital Beijing Beijing China 100032

    Sponsors and Collaborators

    • Peking Union Medical College Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Wen Zhang, Professor, Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT04314323
    Other Study ID Numbers:
    • IRPF group in China
    First Posted:
    Mar 19, 2020
    Last Update Posted:
    Mar 19, 2020
    Last Verified:
    Mar 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by Wen Zhang, Professor, Peking Union Medical College Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 19, 2020