TCTR20210720005招募中2 期
Preliminary study: Safety and Immunological Response following COVID-19 Vaccination in COVID-19 survivors
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 180
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. Males or females at least 18 years of age (inclusive)
- •2. Had a history of SARS-CoV-2-positive by RT-PCR from airway specimens at screening day (10+/-4 weeks or 20+/-4 weeks after detection)
- •3. Can understand Thai language through speaking, reading and writing
- •4. 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 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 received blood transfusion, plasma, blood product, blood components, immunoglobulins, antiviral or antibodies within the last 90 days
- •3. Have history of cigarettes smoking, alcohol drinking and history of drug abuse
- •4. Be pregnant
- •5. Have history of any vaccination within 14 days before screening visit
- •6. Had received more than one COVID-19 vaccination before diagnosis of COVID-19 infection
- •7.Had received any COVID-19 vaccination after Yes
- •diagnosis of COVID-19 infection
- •8. Have unstable disease or could not control the symptom
- •9.Have history of immunodeficiency or use immunosuppressant or steroid drugs?
- •10. Have any unusual symptoms or medical history that considered unable to participate in the study
研究者
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