Chronic Hepatitis B Infection Clinical Trial
Official title:
Quality of Life and Health Utility of Patients With Chronic Hepatitis B Infections
Verified date | October 2017 |
Source | The University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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 estimate the cost-effectiveness of anti-viral treatments resulting
from the prevention of the progression of disease from uncomplicated CHB carriers to
cirrhosis and hepatocellular carcinoma (HCC).
The following hypotheses will be tested:
1. Patients with chronic hepatitis B virus (HBV) have poorer health-related quality of life
(HRQOL) than the general population;
2. Patients with more severe stages of chronic HB infections have lower health related
quality of life and health utility values;
3. Anti-viral treatment can improve the HRQOL and health utility for patients with CHB
infections;
4. The cost-effectiveness of different treatments for chronic HBV infections can be
directly compared in terms of cost/QALY gained.
Status | Completed |
Enrollment | 589 |
Est. completion date | December 2009 |
Est. primary completion date | June 2009 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: Subjects will be included in the study if they: 1. Are 18 years and above in age; 2. Are known to be HBsAg positive for more than six months; 3. 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 Criteria: Subjects will be excluded from the study if they have one of the following: 1. Unable to understand and communicate in Chinese Language; 2. Known cognitive impairment; 3. Diagnosed end-stage non-hepatitis B related chronic illness such as terminal cancer; 4. Patients currently abusing alcohol (>30 units/week) or illegal drugs; 5. Co-infection with HIV, hepatitis C virus (HCV) or hepatitis D virus (HDV); 6. Post-liver transplant; 7. Refuse to give consent. |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Two Regional Hospitals | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong | Hospital Authority, Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | SF-36 Health-related quality of life scores | The Short Form (36) Health Survey is a 36-item, patient-reported survey of patient health. It consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability. | Baseline | |
Secondary | SF-6D Preference-based health utilities | The Short Form-6 Dimension (SF-6D) is a widely used preference-based generic HRQOL measure with a multiattribute classification system consisting of six dimensions: physical functioning, role functioning, social functioning, pain, mental health, and vitality. Each dimension is composed of three to five levels. The SF-6D values range from 0.315 to 1, with higher scores indicating better HRQOL anchoring on the 0 (dead) to 1 (full health) scale. | Baseline | |
Secondary | Quality adjusted life years | To calculate QALYs under different anti-viral treatments that prevent progressions to cirrhosis and HCC, the life expectancy of a person with or without cirrhosis or HCC will be estimated, starting with the age of 18. | Baseline | |
Secondary | Costs of different treatment strategies for HBV infection | Baseline |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04030039 -
Cohort Study of Clinical Outcomes in Chronic HBV Infection Patients With Low HBsAg Under Unplanned Intervention
|
||
Recruiting |
NCT03209011 -
The Changes of CD4+T Cells Frequency and Function During Antiviral Therapy
|
Phase 4 | |
Recruiting |
NCT03208998 -
The Changes of Natural Killer Cells Frequency and Function During Antiviral Therapy
|
Phase 4 | |
Recruiting |
NCT03210493 -
The Changes of Treg Cells Frequency and Function During Antiviral Therapy
|
N/A | |
Recruiting |
NCT03210467 -
The Changes of Plasmacytoid Dendritic Cells Frequency and Function During Antiviral Therapy
|
N/A | |
Recruiting |
NCT03210506 -
The Changes of Cytokines During Antiviral Therapy
|
N/A | |
Recruiting |
NCT03209037 -
The Changes of CD8+T Cells Frequency and Function During Antiviral Therapy
|
Phase 4 | |
Recruiting |
NCT04638439 -
The Safety and Efficacy of Sequential Treatment of Ropeginterferon Alfa-2b (P1101) and Anti-PD1 in Interferon-Naive Adults With Chronic Hepatitis B or D Infection
|
Phase 1 | |
Recruiting |
NCT03587467 -
Study on Gut Microbiota in Chronic HBV Infected Patients
|
||
Completed |
NCT05355467 -
Efficacy and Safety of Ricovir® in Maintaining Durability of Viral Response in Chronic Hepatitis B Patients Who Have Been Treated With Viread® and Have Undetectable HBV DNA in Serum
|
Phase 4 | |
Recruiting |
NCT04135235 -
Effect and Safety of Propofol Fumarate for Mother-to-child Blocking of Hepatitis B
|