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临床试验/NCT04584463
NCT04584463Unknown不适用

Factors Associated With Neurological Prognosis 30 Days After an ICU Admission for a Myocardial Infarction Complicated by an Out-of-Hospital Cardiac Arrest : an Observationnal Multicentric Study

Central Hospital, Nancy, France0 个研究点目标入组 110 人开始时间: 2020年10月30日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
110
主要终点
Neurologic outcome (CPC)

研究概览

简要总结

This study evaluate the association of some in-ICU factors with the neurological prognosis of patients admitted for an out-of-hospital cardiac arrest due to a myocardial infarction.

详细描述

Pre-hospital factors associated with poor neurologic outcome are well known. Meanwhile, in-ICU factors for the first 24 hours may impact neurologic outcome.

This observational study aim to study the factors such as ECLS, NSE dosage, therapeutic hypotermia... and their association with neurologic outcome in patient with myocardial infarction due to instable coronaropathy complicated by an out-of-+hospital cardiac arrest.

This is designed to be a observationnal, prospective, multicentric national french study

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • aged of 18 years old or more
  • non opposition of the patient, or his family if he is unable to consent, after loyal and comprehensive explanation
  • patient admitted in ICU
  • the reason for admission is a resurected out-of-hospital cardiac arrest
  • the cause of the cardiac arrest is a type 1 myocardial infarction

排除标准

  • refractory cardiac arrest (no flow > 30 minutes in normothermia)
  • in-hospital cardiac arrest
  • pregnancy
  • patient under juridic protection
  • opposition of the patient, or of his family is he is unable to consent.

结局指标

主要结局

Neurologic outcome (CPC)

时间窗: 30 day from in-ICU admission

Cerebral Performance Category Scale to assess neurologic outcome 1-2 : good outcome 3-4-5 : bad outcome

次要结局

  • Neurologic outcome (Rankin)(30 day from in-ICU admission)
  • death(30 day form in-ICU admission)

研究者

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Principal Investigator
主要研究者

Pr Bruno LEVY

Professor Bruno LEVY

Central Hospital, Nancy, France

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