EUCTR2021-006172-16-AT进行中(未招募)1 期
Detection and Characterization of Anti-SARS-CoV-2 Salivary Antibodies after COVID-19 Booster Vaccines – The CoVVacBoost Study - The CoVVacBoost Study
Medical University of Graz0 个研究点目标入组 1,200 人开始时间: 2021年11月16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
- 1,200
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
- •Participants must be 18 years or older, able to understand study procedures, provide written informed consent (Biobank informed consent and study specific informed consent), and meet the following inclusion criteria:
- •1. Healthy Individuals who received full vaccination with any authorized COVID-19 vaccine and decided to receive a booster vaccination as recommended by national guidelines.
- •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 1000
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 200
排除标准
- •1.Presence of diseases or therapies that are likely to interfere with the immune response to booster vaccination.
- •2.Any contraindications to the vaccine planned to receive as listed in the product characteristics.
- •3.Lack of willingness to undergo serial blood draws and attend follow-up appointments.
- •4.Having already received a third (booster) vaccination with any COVID-19 vaccine.
- •5.Women who are pregnant or breastfeeding.
- •6.Persons who are not willing to sign the informed consents (biobank informed consent and study specific informed consent)
研究者
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