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临床试验/NCT07665060
NCT07665060进行中(未招募)不适用

Assessing HIV Antibody Increases Following Viral Rebound in People Receiving Antiretroviral Therapy

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 6,100 人开始时间: 2026年4月1日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
6,100
试验地点
1

研究概览

简要总结

The purpose of this study is to establish a proof-of-concept for whether rapid test can detect viral rebounds that occurred within a retrospective time window among PLHIV receiving ART in the United States and sub-Saharan Africa.

The objective of this study is to assess whether HIV antibody levels rise following HIV viral rebound, and the sensitivity and specificity of antibody level increases for detecting HIV viral rebounds.

The investigators will conduct a retrospective matched case-control study of individuals with or without suppressed viral load on antiretroviral therapy (ART). Biobanked specimens will be tested for antibody levels.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

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

入选标准

  • HIV-positive individuals aged 15 or older at the time of ART initiation.
  • Participated in HIV plasma or serum biobanking and viral load testing, with three samples after January 1, 2015 as follows:
  • T1 specimen with suppressed VL and sufficient sample to conduct antibody testing.
  • T2 specimen collected 1-13 months after T1, with: Cases: unsuppressed VL; Controls: suppressed VL.
  • T3 specimen collected 1-13 months after T2, with sufficient sample to conduct antibody testing.
  • At least one VL measurement recorded prior to T1, with:
  • All VL measurements made in the year prior to T1 showing suppressed VL.
  • If no VL measurements were made in the year prior to T1, the most recent VL measurement made prior to T1 showing suppressed VL.

排除标准

  • Individuals with advanced HIV disease from 1 year prior to T1 until T3, defined as:
  • CD4 cell count <200 cells/mm
  • Any AIDS-defining illnesses.
  • Individuals with severe illness or hospitalization from 1 year prior to T1 until T
  • Individuals with immune disorder or cancer diagnosis from 1 year prior to T1 until T
  • Individuals with known recent infection at time of ART initiation (ART initiated within 1 year of estimated date of detectable infection).
  • Individuals known to have been infected with HIV perinatally.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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