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临床试验/NCT01831843
NCT01831843已完成不适用

Effect of Breathing Circuits on Intraoperative Body Temperature

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 111 人开始时间: 2013年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
111
试验地点
1
主要终点
trend of changes on body temperature

研究概览

简要总结

To evaluate differences in intraoperative body temperature between heated huimid breathing circuit and conventional breathing circuit

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •aged 18-70 years,
  • •ASA I or II
  • •patients scheduled for craniotomy under general anesthesia

排除标准

  • •ASA III or IV
  • •Duration of anesthesia time less than 4 hours
  • •emergency operation

研究组 & 干预措施

Group C

Placebo Comparator

non-heated, non-humidified conventional breathing circuit was used in group C patient

干预措施: Group C (Device)

Group E

Experimental

breathing tube which apply humidity and heat (Evaqua™ Breathing Circuits manufactured by Fischer & Paykel)was used in group E patient

干预措施: Group E (Device)

Group M

Experimental

Heated humid tube with a warming device (Mega Acer kit manufactured by Acemedical,Seoul Korea)was used in group M patient

干预措施: Group M (Device)

结局指标

主要结局

trend of changes on body temperature

时间窗: from the point of postintubation up to 5 hours

Investigate differences on core body temperature among different kinds of circuit (heated-humid circuit, humid circuit, conventional circuit)

次要结局

  • total duration of airwarmer(Bair-Hurgger warming unit) using time(from the point of postintubation up to 5hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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