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临床试验/NCT00000262
NCT00000262已完成不适用

Effects of Combined Sevoflurane and Nitrous Oxide Inhalation

University of Chicago1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 1996年11月最近更新:
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
20
试验地点
1
主要终点
Pain intensity, pain bothersomeness

研究概览

简要总结

The purpose of this study is to determine the effects of combined sevoflurane and nitrous oxide inhalation on mood, psychomotor performance, and the pain response in humans.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Care Provider)

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Placebo +/- 30% Nitrous oxide

Placebo Comparator

干预措施: 30% Nitrous oxide (Drug)

Placebo +/- 30% Nitrous oxide

Placebo Comparator

干预措施: Placebo (Other)

Sevoflurane 0.2% +/- 30% Nitrous oxide

Active Comparator

干预措施: 30% Nitrous oxide (Drug)

Sevoflurane 0.2% +/- 30% Nitrous oxide

Active Comparator

干预措施: 0.2% sevoflurane (Drug)

Sevoflurane 0.4% +/- 30% Nitrous oxide

Active Comparator

干预措施: 30% Nitrous oxide (Drug)

Sevoflurane 0.4% +/- 30% Nitrous oxide

Active Comparator

干预措施: 0.4% Sevoflurane (Drug)

结局指标

主要结局

Pain intensity, pain bothersomeness

时间窗: During inhalation

Inhalation was for 68 min divided into 4 blocks with nitrous oxide added during either block 2 or block 4

Mood

时间窗: During inhalation

Inhalation was for 68 min divided into 4 blocks with nitrous oxide added during either block 2 or block 4

Psychomotor performance

时间窗: During inhalation

Inhalation was for 68 min divided into 4 blocks with nitrous oxide added during either block 2 or block 4

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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