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临床试验/EUCTR2010-022641-25-NL
EUCTR2010-022641-25-NL进行中(未招募)不适用

Maraviroc Abacavir STudy – effect on Endothelial Recovery - MASTER

niversity Medical Center Utrecht0 个研究点目标入组 24 人开始时间: 2011年6月20日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
24

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

  • -Age > 18 years
  • -HIV-1 infection
  • -Treatment with antiretroviral regimen containing abacavir for at least the previous 3 months
  • -Undetectable plasma HIV RNA (50 cp/ml) for at least 6 months (one ‘blip’ allowed, which is defined as a detectable plasma HIV-RNA level between 50 and 400 copies/ml, preceded and followed by undetectable (<50 copies/ml) plasma HIV-RNA measurements)
  • -CD4+ cell count > 200 cells/µL
  • -Signed informed consent
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Pregnancy
  • -Breastfeeding
  • -Allergy for peanuts or soya
  • -Hypersensitivity for maraviroc
  • -Treatment of underlying malignancy
  • -Acute infection in the preceding 30 days
  • -Renal insufficiency requiring hemodialysis
  • -Acute or decompensated chronic hepatitis
  • -Modification of antiretroviral regimen in the previous 3 months

研究者

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