EUCTR2019-000801-61-BE进行中（未招募）1 期
Toward an optimal accelerated Tick-Borne Encephalitis (TBE) vaccination schedule for the last-minute traveler - FASTBEPROTECT
Institute of Tropical Medicine Antwerp0 个研究点目标入组 75 人开始时间: 2019年4月8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
- 入组人数
- 75
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. =18 to =60 years of age at time of inclusion
- •2. Willingness to provide written informed consent
- •3. Personnel members at the Belgian Defense
- •4. Prepared to follow the study schedule
- •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 75
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Seropositive for TBE (tested during screening visit).
- •2. Subjects with a known allergy to one of the components of the vaccine
- •3. Immune depressed subjects or subjects who take immunodepressant and/or –stimulant medication
- •4. Planned land deployment to TBE endemic regions during the study period
- •5. Ongoing pregnancy or active child wish (for female subjects)
- •6. Planned vaccination with an inactivated vaccine within 2 weeks before or after each vaccination or with a live attenuated vaccines within 1 month before or after each vaccination
- •7. Yellow fever vaccination planned within the whole study period
研究者
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