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临床试验/NCT00000251
NCT00000251已完成2 期

Effects of Subanesthetic Concentrations of Isoflurane/Nitrous Oxide

University of Chicago1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 1994年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
10
试验地点
1
主要终点
Logical reasoning test

研究概览

简要总结

The purpose of this study is to conduct experiments to examine subjective and reinforcing effects of nitrous oxide. Mood altering and psychomotor effects will be tested on non-drug abusers and preference procedures will be used to assess reinforcing effects. To evaluate the acute and residual effects of subanesthetic concentrations of isoflurane/nitrous oxide combinations in healthy volunteers.

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
Single (Participant)

入排标准

年龄范围
21 Years 至 32 Years(Adult)
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

Placebo Comparator

Subjects inhale 100% oxygen

干预措施: 100% oxygen (Other)

30% N2O

Active Comparator

Subjects inhale 30% N2O

干预措施: 30% N2O (Drug)

0.2% isoflurane

Active Comparator

Subjects inhale 0.2% isoflurane

干预措施: 0.2% isoflurane (Drug)

0.4% isoflurane + 30% N2O

Active Comparator

Subjects will inhale a combination of 0.4% isoflurane and 30% N2O

干预措施: 30% N2O (Drug)

0.4% isoflurane

Active Comparator

Subjects inhale 0.4% isoflurane

干预措施: 0.4% isoflurane (Drug)

0.2% isoflurane + 30% N2O

Active Comparator

Subjects will inhale a combination of 0.2% isoflurane and 30% N2O

干预措施: 30% N2O (Drug)

0.2% isoflurane + 30% N2O

Active Comparator

Subjects will inhale a combination of 0.2% isoflurane and 30% N2O

干预措施: 0.2% isoflurane (Drug)

0.4% isoflurane + 30% N2O

Active Comparator

Subjects will inhale a combination of 0.4% isoflurane and 30% N2O

干预措施: 0.4% isoflurane (Drug)

结局指标

主要结局

Logical reasoning test

时间窗: 15 & 30 min inhalation and 5, 30, & 60 min post inhalation

Free recall memory test

时间窗: 15 & 30 min inhalation and 5, 30, & 60 min post inhalation

Auditory reaction time

时间窗: 15 & 30 min inhalation and 5,30 & 60 min post inhalation

Digit symbol substitution test

时间窗: 2,15 & 30 min inhalation and 5,30 & 60 min post inhalation

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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