TCTR20230406002已完成4 期
Immunity Against SARS-CoV-2 (COVID-19) and Safety Following Evusheld (Long-acting Antibody) in Immunocompromised Children and Adolescents
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 70
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 6 Years 至 18 Years(—)
- 性别
- All
入选标准
- •1. Males or females 5 - < 18 years of age and weights more than or equal 20 kg(s).
- •2. Participants in a research with immune deficiency and symptoms were stable, classified as malignant or non-malignant.
- •3. Participants or guardian of participant understand(s) Thai language through speaking, reading and writing
- •4. Participants or guardian of participant be able
- •to communicate through electronic tools such as Google form or line.
- •5. Capable of attending all study visits according to the study schedule.
- •6. Capable of informed assent/consent and provision of written informed consent before any study procedures
排除标准
- •1. Have history of severe drug or vaccine allergy (anaphylaxis)?
- •2. Have history allergic to the components of the
- •3. Participant has an infection or who has the
- •history of COVID-19 infection within the last 90 days? or who has at higher risk of getting COVID-19
- •4. Did not receive any vaccine COVID-19 within 12
- •weeks before the enrollment?
- •5. Have any symptoms of acute illness within 3 days
- •before the enrollment?
- •6. Be pregnant?
研究者
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