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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04371276
Other study ID # 17160962
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date May 31, 2022

Study information

Verified date February 2023
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Immunisation policies have strong influences on the epidemiology of hepatitis A and B infection. In Hong Kong, vaccines against both viruses have been available through different channels and programmes in the past 3 decades. To evaluate the changes in the prevalence of hepatitis A and B in the general population, a seroepidemiology study is conducted involving a prospective cross-sectional survey followed for serology testing. Eligible members of 1327 spatially random households would be invited to join the study by completing a questionnaire and providing blood samples, either by dried blood spots or venesection, for determining the presence of antigen and/or antibody against hepatitis B, as well as antibody against hepatitis A. The main measures comprise a set of metrics on the prevalence of hepatitis A and B. Analysis would be conducted to examine the association of risk factors with the tested markers and describe the attitudes towards viral hepatitis vaccination. The results would allow us to understand the transmission potential of hepatitis A and B in the community would be influenced by the changing disease epidemiology and coverage of vaccination, which inform the development of new vaccination strategies in Hong Kong


Recruitment information / eligibility

Status Completed
Enrollment 2888
Est. completion date May 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - residents normally living in Hong Kong - living in domestic households randomly selected from Building Groups - Any age, while subjects below the age of 18 would require informed consent of their guardians for participation - Any gender Exclusion Criteria: - unable to understand written Chinese or English, - failure to give consent for participation - living in institution or non-domestic housing, - foreign domestic helpers, - normally living in Hong Kong

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
Blood samples will be collected from recruited subjects from invited households for testing for hepatitis B (HBsAg, anti-HBs and anti-HBc) and hepatitis A (anti-HAV)

Locations

Country Name City State
China Prince of Wales Hospital Hong Kong Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary hepatitis B infection prevalence Proportion of individuals with positive HBsAg 12 months
Primary hepatitis A immunity prevalence Proportion of individuals with positive IgG against HAV 12 months
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