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临床试验/TCTR20210517006
TCTR20210517006招募中2 期

Immunogenicity and the safety of the COVID-19 vaccines available in Thailand.

Chulabhorn Royal Academy0 个研究点目标入组 3,000 人开始时间: 2021年5月17日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
3,000

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
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. 18 years old or more
  • 2. negative for blood SARS-CoV-2 antibody
  • 3. negative for nasopharynx PCR for SARS-CoV-2
  • 4. Negative urine pregnancy test (in case of potential of pregnancy)
  • 5. No history of a severe allergic reaction to the prior vaccine.
  • 6. No fever nor history of fever within 14 days.
  • 7. No symptom of respiratory tract infection within 14 days.
  • 8. ECOG 0,1
  • 9. sign informed consent to the study.

排除标准

  • 1. prior COVID-19 vaccination.
  • 2. Vaccination with any vaccines within 30 days
  • 3. administration of steroid or receive immunoglobulins within 30 days
  • 4. Receive immunosuppression agent within 30 days.
  • 5. pregnancy.
  • 6. lactation.
  • 7. acute coronary syndrome in the past year.
  • 8. Acute stroke in the past year.
  • 9. Splenectomy
  • 10. active chronic infectious disease.

研究者

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