Status:

COMPLETED

Quality of Life and Health Utility of Patients With CHB Infections

Lead Sponsor:

The University of Hong Kong

Collaborating Sponsors:

Hospital Authority, Hong Kong

Conditions:

Chronic Hepatitis B Infection

Eligibility:

All Genders

18+ years

Brief Summary

The aim of the study is to assess the health-related quality of life (HRQOL) and preference-based health utilities of chronic hepatitis B (CHB) carriers in different stages of illness. It will also es...

Detailed Description

Design, Setting \& Subjects: A cross-sectional study and biomathematical modelling will be carried out. In the cross-sectional study, patients known to CHB carriers will be identified from the registr...

Eligibility Criteria

Inclusion

  • Subjects will be included in the study if they:
  • Are 18 years and above in age;
  • Are known to be HBsAg positive for more than six months;
  • Can be classified into one of the following sages of liver diseases:
  • (i) Uncomplicated CHB: Patients with chronic CHB infections but normal liver function and without cirrhosis or HCC.
  • (ii) CHB with impaired liver function or compensated cirrhosis, not on anti-viral treatment.
  • (iii) CHB with impaired liver function or compensated cirrhosis, on anti-viral treatment.
  • (iv) Decompensated cirrhosis: Patients with CHB infection and cirrhosis complicated by one or more of the following: variceal bleeding, hepatic encephalopathy or ascites.
  • (v) Hepatocellular Carcinoma: Patients with confirmed diagnosis of HCC
  • d. Have given written consent to take part in the study.

Exclusion

  • Subjects will be excluded from the study if they have one of the following:
  • Unable to understand and communicate in Chinese Language;
  • Known cognitive impairment;
  • Diagnosed end-stage non-hepatitis B related chronic illness such as terminal cancer;
  • Patients currently abusing alcohol (\>30 units/week) or illegal drugs;
  • Co-infection with HIV, hepatitis C virus (HCV) or hepatitis D virus (HDV);
  • Post-liver transplant;
  • Refuse to give consent.

Key Trial Info

Start Date :

November 1 2006

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 1 2009

Estimated Enrollment :

589 Patients enrolled

Trial Details

Trial ID

NCT03329820

Start Date

November 1 2006

End Date

December 1 2009

Last Update

November 6 2017

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Two Regional Hospitals

Hong Kong, Hong Kong