NCT04446286已完成不适用
Bicentric Study on the Use of ECMO-VV or VA for Severe ARDS Associated With Covid-19
University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年6月18日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Retrospective description of effect of the ECMO-VV or ECMO-VA in the management of severe ARDS refractory in patients of the Strasbourg and Louvain centres with covid-19
研究概览
简要总结
Describes the cohort of patients receiving ECMO-VV or ECMO-VA in the management of severe ARDS refractory to SARS-CoV-2 in the Strasbourg and Louvain centres
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Other
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
- •Patient over the age of 18;
- •Diagnostic COVID-19 by RT-PCR;
- •Hospitalisation in resuscitation for the management of complications related to COVID-19
- •Implanted ECMO-VV or VA during hospitalisation;
- •Patient agreeing to participate in the study
排除标准
- •Sujet who has expressed opposition to participating in the study.
- •Sujet under guardianship or trusteeship
- •Sujet under safeguard of justice
结局指标
主要结局
Retrospective description of effect of the ECMO-VV or ECMO-VA in the management of severe ARDS refractory in patients of the Strasbourg and Louvain centres with covid-19
时间窗: files analysed retrospectily from March 1st, 2020 to August 1st, 2020 will be examined
次要结局
未报告次要终点
研究者
研究点 (1)
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