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临床试验/NCT03510013
NCT03510013已完成不适用

1-1-8 Wash-in for Sevoflurane Low Flow Anesthesia

Khon Kaen University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2018年4月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
Time

研究概览

简要总结

The investigators propose a new wash-in technique for sevoflurane low flow anesthesia with fresh gas flow of O2:N2O or O2:air 1:1 L/min with sevoflurane 8%.

The objective of this study is to identify time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5%

详细描述

The benefits of low flow anesthesia are economic, less pollution, more heat and humidity preservation but it requires appropriate wash-in phase. The current wash-in protocols for sevoflurane are complicated and time consuming. The investigators propose a new 1-1-8 sevoflurane wash-in protocol which is more simple and predictable.

The objective of this study is to identify time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5% with 1-1-8 wash-in protocol.

All patients will receive iv propofol 2 mg/kg as induction agent and succinyl choline 1.5 mg/kg for intubation. Then the ventilation will be controlled to achieve end-tidal CO2 30-35 mmHg with O2:N2O or O2:air 1:1 L/min with sevoflurane 8%. Time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5% will be recorded and analyzed. After that, the concentration of sevoflurane and anesthetic technique will be adjusted to requirement of anesthesiologist.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ASA classification I-II
  • age 18-65 years

排除标准

  • BMI > 35
  • contraindicated for N2O
  • • with pulmonary or cardiac disease

研究组 & 干预措施

1-1-8 wash-in

Experimental

Wash-in using O2:N2O or O2:air 1:1 L/min with sevoflurane 8%

干预措施: 1-1-8 wash-in (Procedure)

1-1-8 wash-in

Experimental

Wash-in using O2:N2O or O2:air 1:1 L/min with sevoflurane 8%

干预措施: Sevoflurane (Drug)

结局指标

主要结局

Time

时间窗: participants will be followed until alveolar concentration of sevoflurane reaches 3.5%, as expected of 10 minutes

Time (in second) to achieve alveolar concentration of sevoflurane 1, 1.5, 2, 2.5, 3, and 3.5%

次要结局

  • Heart rate(participants will be followed until alveolar concentration of sevoflurane reaches 3.5%, as expected of 10 minutes])
  • Blood pressure(participants will be followed until alveolar concentration of sevoflurane reaches 3.5%, as expected of 10 minutes])

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thepakorn Sathitkarnmanee

Associate Professor

Khon Kaen University

研究点 (1)

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