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临床试验/NCT02426255
NCT02426255招募中不适用

Prospective Cohort of Severe Trauma Patients Hospitalized in West French Intensive Care Units

Nantes University Hospital5 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2013年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
5,000
试验地点
5
主要终点
in ICU stay complications

研究概览

简要总结

The purpose of this observational epidemiological study is to investigate the management and the complications associated with severe trauma. Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

详细描述

Pseudonymized data will be collected by study coordinators in a secured e-database.

Cross audit will be performed to check data.

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
15 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • severe trauma
  • and/or traumatic brain injury
  • and/or hemorrhage

排除标准

  • Consent withdrawal

结局指标

主要结局

in ICU stay complications

时间窗: Within the 28 first days after ICU admission date

Nosocomial Infections (epidemiology, risk factors, antibiotic susceptibility of pathogens) Organ failures (incidence, risk factors) Bleeding, hemorrhage Intra-cranial hypertension, brain ischemia Mechanical ventilation weaning, extubation failure

次要结局

  • Duration of mechanical ventilation(in ICU (up to 90 days))
  • ICU length of stay(in ICU (up to 90 days))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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