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临床试验/TCTR20230406002
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

Faculty of Medicine Siriraj Hospital, Mahidol University0 个研究点目标入组 70 人开始时间: 2023年4月6日最近更新:
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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