EUCTR2020-005984-29-NL进行中（未招募）1 期
[89Zr]Df-IAB22M2C anti-CD8 minibody PET/CT imaging to assess the in vivo distribution of CD8+ T-cells in COVID-19 patients
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •All patients must meet all of the following criteria:
- •1. microbiologically proven SARS-CoV-19 infection;
- •2. More than or equal to 18 years of age;
- •3. Ability to provide written informed consent.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •A patient will be excluded from participation in the trial if one or more of the following criteria are met:
- •1. Contra-indication for PET; pregnancy, breast-feeding, severe claustrophobia
- •2. Contra-indication for administration of iodine-containing contrast agents
- •3. Other serious illness, e.g. history of malignancies or auto-immune disorders
- •4. Known pre-existing lymphopenia from an unrelated other medical condition
- •5. Estimated creatinine clearance = 30mL/min according to the Cockcroft-Gault formula (or local institutional standard method) OR oligo-uric patients (<400mL/24hr)
研究者
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终止
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