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临床试验/NCT03594318
NCT03594318招募中不适用

Versailles Hospital Cardiac Arrest Registry

Versailles Hospital1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
1
主要终点
Long term favorable outcome

研究概览

简要总结

Out-of-hospital and in-hospital cardiac arrest (CA) requiring intensive care unit management.

Data collection using a standardized form : demographic data and data related to the CA according to the Utstein guidelines.. Circumstances of onset, dates and times of onset and control of abnormal movements (myoclonus and.or seizures).

On-scene clinical findings, pre-hospital and hospital care providers, timing of various treatments and supportive care, results of etiological investigations, cause of CA. Dates and times of EEG monitoring, EEG results. Outcomes including vital status and Cerebral Performance Category scale score at ICU and hospital discharge, day-90 and 1-year after CA and determined based on data in the ICU and/or hospital/neurologist charts and/or general practitionner phone interview.

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

  • Cardiac arrest requiring Intensive Care Unit management
  • Age >= 18 years

排除标准

  • Refusal to participate

结局指标

主要结局

Long term favorable outcome

时间窗: 1 year

A favorable outcome is defined by a Cerebral Performance Category scale score (CPC) of 1 or 2. The Cerebral Performance Category scale score will be determined according to hospital charts and/or general practitioner phone interview. The CPC score : \[5: Death, 4: Persistent vegetative state, 3: Severe disability, 2: Moderate disability, 1 : Low disability\]

次要结局

  • Short term favorable outcome(3 months)
  • Complications of anticoagulant/ antiplatelet therapies(28 days)
  • Long term quality of life as assessed by the Short Form (36) Health Survey (SF36)(1 year)
  • Postanoxic Status Epilepticus(28 days)
  • Short term quality of life as assessed by the Short Form (36) Health Survey (SF36)(3 months)

研究者

发起方
Versailles Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

LEGRIEL stephane

study principal investigator

Versailles Hospital

研究点 (1)

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