Hepatitis Inequalities Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChinese University of Hong Kong

About this trial

Health inequality in liver diseases including age, gender, ethnicity and socioeconomic status has been increasingly recognised and potentially hinder hepatitis elimination. Health inequality has significant impact to evaluate the impact diagnostic and treatment uptake rates of chronic viral hepatitis on risk of hepatocellular carcinoma (HCC), hepatic event and liver-related death in patients with chronic hepatitis B and/or C. To overcome the limitation of small prospective cohort study of limited recruitment period, retrieving information from the Clinical Data Analysis and Reporting System (CDARS) from Hospital Authority (HA) will be one of the best way to answer these questions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients will be eligible if they have any of these viral markers (HBeAg / HBsAg / HBV DNA / HCV RNA) and/or any of the following diagnosis codes (ICD-9 070-070.9; 348.3, 349.82, 456, 456.2, 456.8, 567.2, 567.8, 570, 571.2, 571.5, 571.6, 572.2, 572.3, 572.4, 789.5) checked or coded in any public hospitals or clinics from 1 January 2000 to 31 March 2024.

Disqualifiers

Patients with missing age, gender, ethnicity and socioeconomic status

(Subgroup analysis for ethnicity and socioeconomic status) Patients with missing ethnicity and socioeconomic status

Serious medical illnesses or malignancy with life expectancy <1 year

Trial population

From the Clinical Data Analysis and Reporting System (CDARS) from Hospital Authority

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Safety

Time from diagnosis of hepatitis to treatment.

Time frame
From 1 January 2000 to 31 March 2024

Secondary outcomes

1

Safety

The composite endpoints of recurrence of hepatic events (e.g. HCC hepatic coma, portal hypertension, variceal bleeding, hepatorenal syndrome).

Time frame
From 1 January 2000 to 31 March 2024

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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