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临床试验/NCT01940861
NCT01940861Unknown不适用

Cerebral Oxymetry in Traumatic Brain Injury

Oslo University Hospital1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2014年11月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
15
试验地点
1
主要终点
Dosage of vasopressor

研究概览

简要总结

Vasopressor for current treatment protocols for acute traumatic brain injury can lead to vasoconstriction and thus cerebral hypoperfusion that can be detected with cerebral oxymetry as a drop in SCO2.

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with acute traumatic severe brain injury requiring neuro intensive care.
  • The patient admitted must be at least 18 years of age and under 60 years.
  • Intoxication is not an obstacle for inclusion as we believe this will not affect the recording in relation to our problem.

排除标准

  • Traumatic injury in the frontal lobes corresponding to the area where ScO2 monitored.
  • Patients in pharmacological studies.
  • Patients with severe heart / lung / blood vessel diseases.

结局指标

主要结局

Dosage of vasopressor

时间窗: 24 hours

次要结局

未报告次要终点

研究者

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

研究点 (1)

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