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临床试验/NCT03434821
NCT03434821已完成不适用

Impact of Hyperoxemia on Incidence of Ventilator-associated Pneumonia

University Hospital, Lille1 个研究点 分布在 1 个国家目标入组 534 人开始时间: 2018年3月15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
534
试验地点
1
主要终点
VAP occurrence

研究概览

简要总结

The aim of this prospective cohort single-center observational study is to determine the impact of hyperoxemia on ventilator-associated pneumonia (VAP) occurrence.

  • SpO2 will be continuously recorded in order to determine the percentage of time spent with hyperoxemia.
  • Patients with VAP will be prospectively identified.
  • Patient characteristics and risk factors for VAP will be prospectively collected.
  • Oxidant stress will be prospectively investigated in study patients: glutathion peroxidase (GPX), plasmatic superoxyde dismutase (SOD), total plasmatic antioxidant status (SAT) and urinary 8-isoprostanes will be performed at ICU admission, once a week, and at VAP occurrence.

Patients with VAP will be compared with those with no VAP

研究设计

研究类型
Observational
观察模型
Other
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

  • Adult patients admitted to the ICU
  • Expected duration of mechanical ventilation > 48h
  • Signed informed consent
  • Social insurance

排除标准

  • Pregnancy or breast feeding
  • No informed consent
  • Hyperbaric oxygen treatment
  • Prisoners and patients under guardianship

结局指标

主要结局

VAP occurrence

时间窗: 28 days after ICU admission

hyperoxemia at ICU admission (PaO2 \>120 mmHg)

次要结局

  • percentage of time spent with hyperoxemia during ICU stay, and the presence of acute lung injury(28 days after ICU admission)
  • percentage of time spent with hyperoxemia during ICU stay(28 days after ICU admission)
  • relationship between hyperoxemia at ICU admission and the presence of acute lung injury (ALI)(28 days after ICU admission)

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (1)

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