CAMERA: Autoimmune Hepatitis Cohort in China

Sponsor
Shanghai Jiao Tong University School of Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT05785793
Collaborator
(none)
1,000
1
60
16.7

Study Details

Study Description

Brief Summary

The goal of this observational study is to describe the clinical features and long-term prognosis in patients diagnosed with autoimmune hepatitis (AIH) in China and assess the effectiveness and safety of AIH treatment options in a real-world setting.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Autoimmune hepatitis (AIH) is a chronic autoimmune liver disease that causes liver inflammation and necrosis, ultimately leading to cirrhosis and liver failure. Although relatively rare, the prevalence of AIH in China has been increasing in recent years, highlighting its significance as a public health issue. However, due to the wide variability in the clinical presentation and outcomes of AIH, diagnosing and managing the disease can be challenging. Moreover, our understanding of the epidemiology, clinical features, diagnosis, and treatment of AIH in China is still limited.

    To address this gap in knowledge, the investigators are conducting the Chinese AIH Cohort study, which collects data from approximately 20 sites across China on treatment progress and success in clinical routine. The study aims to evaluate the effectiveness and safety/tolerability of different AIH treatment options, including standard therapy, and second and third-line treatment options. The investigators also record the long-term prognosis of patients with AIH, tracking whether they achieve remission, require liver transplantation, or experience mortality. Risk factors associated with long-term prognosis and survival will be analyzed to provide insights that can improve the diagnosis, treatment, and management of AIH in this population.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    1000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Other
    Official Title:
    Clinical Characteristics and Outcomes of Autoimmune Hepatitis: a Retro-prospective Multicenter Cohort in China
    Actual Study Start Date :
    Feb 1, 2023
    Anticipated Primary Completion Date :
    Feb 1, 2028
    Anticipated Study Completion Date :
    Feb 1, 2028

    Outcome Measures

    Primary Outcome Measures

    1. Transplant free survival [From baseline to 60 months after baseline]

      Time to the first occurrence of liver transplant or death from any cause

    Secondary Outcome Measures

    1. Liver-related death [From baseline to 60 months after baseline]

      Time to the first occurrence of liver transplant or death from liver-related cause

    2. Biochemical response [From baseline to 60 months after baseline]

      Proportion of patients who achieve complete biochemical response (normalisation of serum transaminases and immunoglobulin G below the ULN)

    3. Remission [From baseline to 60 months after baseline]

      Proportion of patients who achieve remission (hepatitis activity index<4/18)

    4. Complications [From baseline to 60 months after baseline]

      Occurrence of variceal hemorrhage, ascites, jaundice, encephalopathy and hepatocellular carcinoma

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    14 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥ 14 years

    • Probable or definite diagnosis of autoimmune hepatitis according to the International Autoimmune Hepatitis Study Group criteria

    • Availability of all following essential parameters at the initial diagnosis of AIH: including alanine transaminase, aspartate aminotransferase, total bilirubin, alkaline phosphatase, immunoglobulin G, and platelet count

    • Provide informed consent

    Exclusion Criteria:
    • Have a concomitant diagnosis of primary biliary sclerosis, primary sclerosing cholangitis, immunoglobulin G 4-related cholangitis

    • Have an active infection with hepatitis B virus, hepatitis C virus, hepatitis delta virus, HIV, cytomegalovirus, or Epstein-Barr virus

    • Have a concomitant diagnosis of hepatocellular carcinoma or other malignant diseases before the diagnosis of AIH

    • Considered ineligible to the enrollment in the clinical study by the researcher

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Renji Hospital, School of Medicine, Shanghai Jiao Tong University Shanghai Shanghai China 200001

    Sponsors and Collaborators

    • Shanghai Jiao Tong University School of Medicine

    Investigators

    • Study Chair: Xiong Ma, MD,PHD, Renji Hospital, School of Medicine, Shanghai Jiao Tong University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    maxiong, Director of Gastroenterology and Hepatology, Renji Hospital, Shanghai Jiao Tong University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT05785793
    Other Study ID Numbers:
    • AIH-CH
    First Posted:
    Mar 27, 2023
    Last Update Posted:
    Mar 28, 2023
    Last Verified:
    Mar 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 28, 2023