NCT04841707已完成不适用
Total-Body Parametric 18F-FDG PET of COVID-19
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 13
- 试验地点
- 1
- 主要终点
- BAB permeability assessed
研究概览
简要总结
The primary objective is to measure the change between COVID-19 patients and normal subjects; the secondary objective is to measure the change in COVID-19 patients between baseline and 4-month follow up.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •COVID-19 positive patients will have a previous positive COVID-19 test and radiographic findings, and/or a positive SARS-CoV-2 antibody test and be in early recovery.
- •First PET/CT visit needs to be within 8 weeks of COVID-19 diagnosis.
- •Ability to understand and willingness to sign an informed consent form.
- •Ability to adhere to the study visit schedule and other protocol requirements.
- •All persons ≥18 years of age.
排除标准
- •Pregnant or lactating women.
- •Any condition that would prohibit the understanding or rendering of informed consent.
- •Unable to lie supine for 1-hour imaging with PET.
- •Prisoners.
- •Any comorbidity that, in the opinion of the investigator, could compromise protocol objectives.
研究组 & 干预措施
COVID-19 patients
Experimental
干预措施: uEXPLORER/mCT (Device)
结局指标
主要结局
BAB permeability assessed
时间窗: 1 imaging visit up to 60 minutes
Evaluating if there is a change in BAB permeability assessed by lung FDG K1 for patients with COVID 19
次要结局
- 4 month follow-up PET/CT scan(1 imaging visit up to 60 minutes)
研究者
研究点 (1)
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