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临床试验/NCT02344680
NCT02344680已完成不适用

Liver Fibrosis in Zambian HIV-HBV Co-infected Patients: a Long-term Prospective Cohort Study

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 349 人开始时间: 2015年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
349
试验地点
2
主要终点
Change in liver fibrosis stage

研究概览

简要总结

A cohort of adults with HIV-HBV co-infection will be created in Lusaka, Zambia, to describe the short and long-term (up to 10 years of follow-up) HBV and liver outcomes, including the effectiveness of current therapies, and to identify the risk factors for major endpoints of interest, including HCC and HBV functional cure. This cohort will also create a pool of potential participants for in-depth mechanistic studies and clinical trials of novel HBV cure drugs.

详细描述

Among people with HIV in Africa, liver disease is a neglected area of investigation but is anticipated to become increasingly common as patients live longer due to antiretroviral therapy. In Lusaka, Zambia, we previously (NCT02060162, clinicaltrials.gov) described that HIV-HBV co-infection was the most important liver risk factor. However, in that study, only very short-term outcomes could be assessed. Building on these preliminary results and addressing the need to study HIV-HBV during a longer duration of follow-up, the current protocol will focus exclusively on people with HIV-HBV in Zambia. Zambia is an ideal site for this research as it has ~12% HIV prevalence and 6% HBsAg-positivity among adults nationwide. In fact, ~70% of people with HIV-HBV globally reside in Africa. In the proposed study, we will obtain consent from people with HIV-HBV to participate in an observational cohort study with up to 10 years of follow-up. Standard of care antiviral therapies will be received by participants. More in-depth analysis of liver and HBV viral and serological outcomes will occur. Screening for liver cancer will also occur. This study will provide useful clinical and epidemiological information to health policymakers in Zambia and beyond. It will also provide a platform for the training of health workers in Zambia in HBV clinical management.

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

  • Age 18 years or older
  • Living with HIV infection
  • Living with active HBV infection, defined as any single positive HBsAg assay
  • Naïve to antiretroviral therapy or currently participating in HIV/HBV co-infection in IeDEA-SA

排除标准

  • Unable or unwilling to provide informed consent
  • Planning to relocate out of Lusaka district

研究组 & 干预措施

Adults with HIV-HBV co-infection

Adults with HIV-HBV co-infection who are receiving antiretroviral therapy

干预措施: Anti-HIV Agents (Drug)

结局指标

主要结局

Change in liver fibrosis stage

时间窗: From baseline to 10 years of follow-up

Measure of liver fibrosis using AST-to-platelet ratio index (APRI), Fibrosis 4 (FIB-4) and transient elastography. Ascertainment of potential risk factors including demographics, alcohol use, HIV-related biomarkers, HBV DNA, hepatitis delta virus, and other factors.

次要结局

  • Prevalence of significant liver fibrosis (Metavir F2 or greater)(At enrollment)
  • Prevalence of persistent HBV viremia: Measure HBV DNA at month 24(Month 24)
  • Incidence of hepatocellular carcinoma(From baseline to 10 years of follow-up)

研究者

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

Michael Vinikoor

Assistant Professor

University of Alabama at Birmingham

研究点 (2)

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