EUCTR2008-005800-24-AT进行中（未招募）不适用
Characterisation of humoral and cellular immunity of low- and high-responder after TBE vaccination
Medizinische Universität Wien, Institut für Spezifische Prophylaxe und Tropenmedizin0 个研究点目标入组 84 人开始时间: 2008年9月22日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 84
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
- •Adults (=18 years) of both sexes without upper age limit
- •Willingness to sign written informed consent form
- •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
- •Age: < 18 years
- •Pregnancy or breast feeding
- •prior TBE infection
- •Acute infection at day of inclusion (day 0) (body temperature > 37.9°C )
- •Planned surgery within 2 weeks before/after any scheduled rabies vaccination during the entire study
- •Concomitant medication: systemic cortisone, immune suppressive therapy 4 weeks before or planned medication during the study
- •History of autoimmune disease
- •drug addiction
- •plasma donators
- •administration of other vaccines 4 weeks before/after day 0
- •Administration of immunoglobulins 6 weeks prior to any vaccination or blood donation during the entire study period
- •Specific Immune Therapy (Hypo-/Desensibilization) within 14 days before and after the 2 study vaccination doses.
- •History of any malignant disease 5 years prior to the study entry
- •Any contraindication for the administration of the TBE- or influenza vaccine according to the manufactures information.
研究者
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