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临床试验/EUCTR2015-004427-31-SE
EUCTR2015-004427-31-SE进行中(未招募)不适用

Tenofovir Alafenamide Fumarate (TAF) effect on residual intrathecal immune activation

Gothenburg University0 个研究点开始时间: 2016年1月14日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Stable antiretroviral therapy with TDF/FTC or ABC/3TC + 3rd agent (PI/r, NNRTI, or INI) for more than18 months.
  • 2. Plasma HIV-RNA < 50 copies/mL for more than 12 months.
  • 3. No neurological symptoms or severe neurocognitive impairment.
  • 4. No pre-treatment central nervous system opportunistic infection/tumour or HIV-associated dementia.
  • 5. Lumbar puncture performed in the longitudinal cerebrospinal fluid study (University of Gothenburg) between 6 and 18 months before study entry.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 20
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Not on successful antiretroviral therapy.

研究者

发起方
Gothenburg University

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