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临床试验/NCT00830843
NCT00830843已完成4 期

Inhalatorial Sedation in Patient With SAH Versus Conventional Intravenous Sedation (GAS-SAH)

Azienda Ospedaliera San Gerardo di Monza1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2009年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
13
试验地点
1
主要终点
Cerebral Blood Flow

研究概览

简要总结

Recent study has shown that inhalatory sedation is a practicable, effective and not risky method in Intensive Care Unit. Sevoflurane effect on cerebral system have been described in previous studies: it causes an increasing of cerebral blood flow and a decrease of oxygen cerebral consumption. Clinical strategy for Subarachnoid Hemorrhage is orientated to increase cerebral blood flow to limit vasospasm phenomena after SAH. Scope of this study is to evaluate the Cerebral Blood Flow variation associated to Isoflurane sedation versus conventional sedation with propofol .

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

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

  • diagnosis of aSAH
  • indication to DVE positioning
  • clinical indication to sedation and assisted ventilation
  • indication to ICP and CBF monitoring
  • age > 18

排除标准

  • documented cranial hypertension (ICP>18) not controller by liquor drainage
  • age < 18.

研究组 & 干预措施

Propofol

Active Comparator

Propofol(3-4 mg/kg/ora)administrated for 2 hours.

干预措施: Propofol (Drug)

Isoflurane

Experimental

Isoflurane inhalatorial administration for 2 hours at 0.8-1.0% Minimum Alveolar Concentration

干预措施: Isoflurane (Drug)

结局指标

主要结局

Cerebral Blood Flow

时间窗: after 2 hours of drug administration

次要结局

未报告次要终点

研究者

发起方
Azienda Ospedaliera San Gerardo di Monza
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Giuseppe Citerio

MD

Azienda Ospedaliera San Gerardo di Monza

研究点 (1)

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