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Recruiting NCT04139850

The Establishment of Korean Hepatitis B Patients Cohort

Observational Chronic Hepatitis B

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Discontinuation of antiviral treatment in chronic hepatitis B cohort patients.
Who it may be relevant to
Registry conditions: Chronic Hepatitis B. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

According to the World Health Organization about 1,400,000 deaths reported annually, are related to chronic liver disease. Chronic liver disease is very prevalent in South Korea, placing a large economic burden nationwide. Subsequently, an effective and systematized approach to managing chronic hepatitis is imperative in Korea. The natural history of chronic liver disease differs greatly according to race and ethnicity. However, there is scarcity of epidemic data on chronic hepatitis based on Korean patients. Therefore, the investigators plan to establish a prospective multicenter cohort for chronic hepatitis B based on Korean patients that may be utilized for various future clinical studies on chronic hepatitis B in Korea, and thereby serve as a basis for the establishment and distribution of clinical guidelines for Korean patients with chronic hepatitis B, as part of a nationwide project supported by the Centers for Disease Control (CDC), Korea. The investigators plan to collect more than 2,000 cases per year with 6 months of regular follow-up interval as have been advised by the CDC during 10 years of the study period (from Sep. 2015) from 5 tertiary hospitals located in Korea. The investigators plan to register available cases from those who are available to agree to give written informed consent and provide their blood samples to participate in this study prospectively, according to the inclusion and exclusion criteria.

Interventions

  • Drug Discontinuation of antiviral treatment in chronic hepatitis B cohort patients
    For the selective patients in the cohort with long-term antiviral therapy and with conditions such as HBeAg negative or loss more than one year, antiviral therapy is able to be discontinued with an intensive inspection who agreed to the process. If there are need of this intervention, another multicenter IRB approval will be taken.

Primary outcome measures

  • Development of liver cirrhosis, decompensation or liver cancer [Time frame: Time of registration of patient to cohort complement (10 years)]
Secondary outcome measures (1)
  • Safety and efficacy for patients with or without antiviral therapy [Time frame: Time of registration of patient to cohort complement (10 years)]

Eligibility criteria

Inclusion criteria

  • age above 19 years;
  • CHB diagnosis with more than 6 months of HBsAg positive;
  • Patients who followed up regularly by medical institutions due to CHB;
  • Patients who can be followed up according to the research protocol;
  • Patients who have consented to the written consent of the applicant or guardian.

Exclusion criteria

  • HCC diagnosis before enrollment;
  • Malignant tumor other than HCC within 5 years;
  • Hepatitis C virus or human immunodeficiency virus co-infection;
  • Fatal conditions such as decompensated liver function, end stage renal disease and severe heart failure;
  • not be suitable for the research purpose.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

South Korea · 1 center
  • Department of Internal Medicine, Yonsei University College of Medicine — Seoul

Identifiers

NCT: NCT04139850 · 4-2015-0748

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗