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临床试验/EUCTR2007-001861-14-NL
EUCTR2007-001861-14-NL进行中(未招募)不适用

Multicenter randomized clinical trial in Patients with Juvenile Idiopathic Athritis: Safety and efficacy of vaccination with live attenuated Measles, Mumps, Rubella vaccine - safety and efficacy of MMR vaccination in JIA patients

niversity Medical Center Utrecht0 个研究点开始时间: 2008年2月29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)

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

  • - all subtypes of Juvenile Idiopathic Arthritis (JIA) patients according to ILAR criteria
  • - ages 4 - 9 (this is 2 years after initial MMR and before the scheduled booster, usually given at age 9)
  • - five healthy controls (18-65 years)
  • Are the trial subjects under 18? yes
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Use of Infliximab (Remicade, anti-TNF alpha therapy).
  • - Primary immunodeficiency
  • - Fever less than 48 hour prior to vaccination (here the moment of vaccination will be postponed for 1 month)
  • - Evidence of viral or bacterial infection less than 48hours prior to vaccination (here the moment of vaccination will be postponed for 1 month)
  • - Methylprednisolon pulse therapy less than 1 month prior to vaccination (in these cases, the moment of vaccination will be postponed for 1 month)
  • for healthy controls:
  • -serious adverse events to previous MMR vaccination
  • -Use of immunosuppressive drugs
  • -Primary immunodeficiency
  • -Fever less than 48 hour prior to vaccination (vaccination will be postponed)
  • -Evidence of viral or bacterial infection less than 48hours prior to vaccination (vaccination will be postponed)
  • -Methylprednisolon pulse therapy less than 1 month prior to vaccination (vaccination will be postponed)
  • -Pregnancy
  • -Lactation

研究者

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