跳至主要内容
临床试验/NCT06596213
NCT06596213尚未招募不适用

Overcoming Inequalities in Health to Eliminate Hepatitis - Real-World Evidence from a Territory-Wide Cohort

Chinese University of Hong Kong0 个研究点目标入组 100,000 人开始时间: 2024年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
100,000
主要终点
Safety

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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

结局指标

主要结局

Safety

时间窗: From 1 January 2000 to 31 March 2024

Time from diagnosis of hepatitis to treatment.

次要结局

  • Safety(From 1 January 2000 to 31 March 2024)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Grace Lai Hung Wong

Professor

Chinese University of Hong Kong

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Hepatitis Inequalities Study | 临床试验