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临床试验/NCT07589985
NCT07589985招募中不适用

Hep Mec Cohort in Zambia

University of Alabama at Birmingham3 个研究点 分布在 1 个国家目标入组 390 人开始时间: 2020年9月28日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
390
试验地点
3
主要终点
Change in Intrahepatic Immune Cell Subset Frequencies

研究概览

简要总结

Observational cohort of adults with acute and chronic hepatitis B infection in Zambia, with and without HIV coinfection. Participants join the study at the time of diagnosis and before or at the time when they are starting antiviral treatments and then they are followed up over multiple years to assess changes to their liver and evolution of HBV (and HIV if applicable) infection. All treatments for HBV and HIV are standard per local Ministry of Health guidelines.

研究设计

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

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

  • Must meet the inclusion criteria for one of 5 groups, as follows:
  • Group 1 (rx-naive chronic hbv mono): 18+ years old, HBsAg-positive, HIV-negative, eligible for tenofovir-based therapy, reports taking therapy no more than 7 days (could have previously taken if has stopped >1 year ago).
  • Group 2 (acute hbv mono): 18+ years old, HBsAg-positive, HIV-negative, acute/subacute onset of hepatitis signs and symptoms and ALT >10 times upper limit of normal
  • Group 3 (rx-naive hbv/hiv coinfection): 18+ years old, HBsAg-positive, HIV-negative, eligible for tenofovir-based therapy, reports taking therapy no more than 7 days (could have previously taken if has stopped >1 year ago).
  • Group 4 (rx-experienced coinfection with hbv persistence): 18+ years old, history of chronic HBV infection based on two tests 6 months apart, HIV-positive, at least 4 years of tenofovir-based antiviral therapy, currently HBsAg-positive
  • Group 5 (hbsag loss): 18+ years old, HIV-positive or negative, history of chronic HBV infection based on two tests 6 months apart, Currently HBsAg-negative confirmed by sensitive assay

排除标准

  • Hepatitis C coinfection (antibody-positive and RNA-positive), current or recent (past 6 weeks) pregnancy, decompensated cirrhosis on physical examination, unlikely to remain in Lusaka for study duration

研究组 & 干预措施

Treatment-experienced HBV infection with HBsAg loss

Adults with and without HIV coinfection who have a documented history of chronic HBV infection that subsequently resolved (i.e., HBsAg loss) during antiviral therapy

Treatment-naive chronic HBV monoinfection and eligible for antiviral therapy

Adults who are HBsAg-positive, HIV-positive, eligible for HBV antiviral therapy and has not yet or just started taking therapy

Treatment-naive acute HBV monoinfection

Adults who are HBsAg-positive, HIV-negative, and have the syndrome of acute hepatitis

Treatment-naive HBV/HIV coinfection

Adults who are both HBsAg and HIV positive, and are not yet or just started taking HBV-active ART

Treatment-experienced HBV/HIV coinfection with persistent HBsAg-emia

Adults with HBV/HIV coinfection and persistent HBsAg-emia after at least 4 years of HBV-active ART

结局指标

主要结局

Change in Intrahepatic Immune Cell Subset Frequencies

时间窗: Baseline and 1 year

Percentage of immune cell subsets (CD4+ T cells, CD8+ T cells, B cells, NK cells, Macrophages, and Neutrophils) among total liver immune cells as measured by single-cell RNA sequencing. Comparisons will be made between acute and chronic HBV infection, with and without HIV coinfection, and before and after nucleoside analog antiviral therapy.

Number of Differentially Expressed Hepatic Genes Associated with HBsAg Reduction/Loss

时间窗: Baseline and 1 year

Count of genes showing differential expression (fold change ≥2.0, adjusted p-value \<0.05) by single-cell RNA sequencing in liver biopsies from participants achieving HBsAg loss compared to those without HBsAg loss. Gene expression will be analyzed at baseline (predictive analysis), longitudinally (trajectory analysis), and at end of follow-up. Analysis will include comparison across acute vs. chronic HBV infection and with vs. without HIV coinfection.

次要结局

  • HBV viral suppression(Baseline, 1 year, 2 years, 3 years, 4 years, and 5 years)
  • HIV viral suppression(Baseline, 1 year, 2 years, 3 years, 4 years, and 5 years)
  • HBsAg seroclearance(Through study completion, an average of 5 years)
  • HBeAg seroconversion(Through study completion, an average of 5 years)

研究者

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

Michael Vinikoor

Professor of Medicine

University of Alabama at Birmingham

研究点 (3)

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