NL-OMON22289已完成不适用
Investigating the immune response to COVID-19 vaccination in lung transplantation patients (COVALENT study)
niversity Medical Center Groningen (UMCG)0 个研究点目标入组 180 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 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
- Observational
入排标准
入选标准
- •? All patients should be eligible for COVID-19 vaccination as described by the instructions of the manufacturer.
- •? Provision of written informed consent
- •? =18 years of age
- •? Belong to one of the four populations as named in 4.1.
排除标准
- •? Contra-indications for vaccination (unrelated to the study)
- •-History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (e.g., anaphylaxis) to any component of the study intervention(s).
- •-Pregnancy at the time of the vaccinations
- •? Exclusion specific to this investigation
- •-No administration of SARS-CoV-2 vaccine due to any reason
- •-Active (hematological) malignancy
- •-Inherited immune deficiency
- •-Receiving anti-retroviral medication o Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection.
- •-Waitlist patients with a passed COVID-19 infection.
- •-Transplantation candidates who do not receive a transplantation within 15 months after receiving the second vaccination dose will remain included as controls. However, sampling will not continue after long
- •transplantation if the transplant occurs at a later time.
研究者
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