NCT04348448终止不适用
Observational Study on the Use of Canakinumab Administered Subcutaneously in the Treatment of Patients With COVID-19 Pneumonia
AUSL Romagna Rimini1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年2月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- intensive care treatment
研究概览
简要总结
The study is configured as a retrospective and prospective observational study. The study will be multi-center and will involve all COVID-19 pneumonia patients treated with canakinumab administered subcutaneously.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 100 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •patients with COVID 19 who have received or are candidates to receive treatment with canakinumab subcutaneously
- •Age> 18 years
- •Pneumonia diagnosed with Chest X-ray / or Chest CT
排除标准
- •Patients with Covid19-related pathology in the context of another cause of major admission (trauma, surgery)
结局指标
主要结局
intensive care treatment
时间窗: 9 months
percentage of patients treated with canakinumab sc who do not require intensive care treatment during hospitalization for COVID-19
次要结局
- % died after 1 month after treatment(9 months)
- ICU stay times(9 months)
- hospitalization(9 months)
- adverse event(9 months)
研究者
研究点 (1)
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