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临床试验/EUCTR2006-001806-94-BE
EUCTR2006-001806-94-BE进行中(未招募)不适用

Comparison of the efficacy of pneumococcal and tetanus vaccination between hemodialysis patients and renal tranpslant recipients treated with Mycophenolic acid(VACC-IR) study. - VACC-IR

Hôpital Erasme0 个研究点目标入组 90 人开始时间: 2006年5月2日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
90

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- adult patient aged between 18 and 75 years
  • 2- patients transplanted between 1 and 5 years previously; with a kidney graft only, or dialyzed patients registred on the waiting list for a kidney transplant (or with ongoing registration)
  • 3- renal transplant recipients treated with mycophenolic acid and a calcineurin inhibitor for at least 3 months
  • 4- renal transplant recipients who did not experience a rejection episode during the last 6 months, and have stable renal fonctuion for the last 5 months
  • 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

  • 1- no pneumonia or severe infection during 1 mont before vaccination
  • 2- no pneumococcal or tetanos vaccination during the last 5 years
  • 3-no Ivig (intravenous immunoglobulins) treatment during the last 3 months

研究者

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