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临床试验/EUCTR2011-002071-42-ES
EUCTR2011-002071-42-ES进行中(未招募)1 期

Effects of losartan and antiretroviral regimen containing raltegravir in fibrosis inflammation mediators, cardiovascular risk and neurocognitive disorders in HIV infected patients previously effectively treated. - N/A

Fundació Clínic de Recerca Biomèdica0 个研究点开始时间: 2012年1月11日最近更新:
适应症
相关药物

试验速览

阶段
1 期
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. Patients older than 18 years.
  • 2. Patients with HIV infection in antiretroviral treatment with EFV / FTC / TDF with undetectable viral load (VL <37 copies) for at least 48 weeks.
  • 3. Nadir CD4 +> 250 cells/mm3.
  • 4. Patients, properly informed, give their written consent to participate in the study.
  • 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 48
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Criteria for patients with AIDS.
  • 2. Patients with active opportunistic diseases.
  • 3. Patients coinfected with HCV.
  • 4. Patients without tonsillar tissue.
  • 5. Treatment with other drugs receptor antagonists or angiotensin II converting enzyme inhibitors, angiotensin II.
  • 6. Kidney failure.(Glomerular Filtration Rate (GFR < 60 mL/mn)
  • 7. Severe liver failure (PT> 60% ).
  • 8. Pregnant women
  • 9. Known hypersensitivity or contraindication to any study drug.
  • 10. determination of blood pressure (BP) <100/60 mmHg
  • 11. Hyponatremia with serum Na numbers <132 Meq / l
  • 12. History of chronic vomiting the last 6 months
  • 13. History of chronic diarrhea the last 6 months

研究者

发起方
Fundació Clínic de Recerca Biomèdica

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