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临床试验/NCT05154071
NCT05154071已完成不适用

Impact of the Implementation of a Referral Veno-venous Extracorporeal Membrane Oxygenation Centre on Mortality

Centre Hospitalier Universitaire Dijon1 个研究点 分布在 1 个国家目标入组 172 人开始时间: 2021年10月1日最近更新:
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
172
试验地点
1
主要终点
Mortality rate

研究概览

简要总结

Current evidence suggest that regrouping patient supported by veno-venous ECMO in high-volume centre could improve outcome. A dedicated ECMO unit was implemented in Dijon.

The objective of the present study was to evaluate the implementation of this unit. The hypothesis was that patient taken care within this structured care system would have lower mortality.

This research comprises a retrospective observational study conducted in Dijon university hospital

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patient in an adult Dijon ICUs supported by veno-venous ECMO
  • patient hospitalized between January the 1st 2011 and June the 30th 2021

排除标准

  • Refusal to participate,
  • patient admitted to pediatric ICU

研究组 & 干预措施

ECMO VV without dedicated unit

Patient having benefited from an ECMO without the structured care unit

干预措施: Collection of medical data (Other)

ECMO VV dedicated unit

Patient having benefited from an ECMO within the structured care unit

干预措施: Collection of medical data (Other)

结局指标

主要结局

Mortality rate

时间窗: 90 days

次要结局

  • Rate of ECMO adverse events(through study completion, an average of 3 years)
  • Hospital length of stay(through study completion, an average of 3 years)
  • ICU length of stay(through study completion, an average of 3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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