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临床试验/NCT00000259
NCT00000259已完成不适用

Sevoflurane vs Nitrous Oxide Inhalation at Subanesthetic Concentrations

University of Chicago1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 1996年8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
12
试验地点
1
主要终点
Pain intensity

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. Comparisons between nitrous oxide, opiates, and benzodiazepine antagonists will be made. To examine sevoflurane versus isoflurane inhalation at subanesthetic concentrations on mood, pain, and psychomotor performance.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
盲法
Double (Participant, Investigator)

入排标准

年龄范围
21 Years 至 39 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

0.3% sevoflurane

Active Comparator

干预措施: 0.3 % Sevoflurane (Drug)

Placebo

Placebo Comparator

Subject inhales no drug (100% oxygen)

干预措施: Placebo (Other)

0.6% sevoflurane

Active Comparator

干预措施: 0.6% Sevoflurane (Drug)

15% Nitrous oxide

Active Comparator

干预措施: 15 % Nitrous oxide (Drug)

30% Nitrous oxide

Active Comparator

干预措施: 30% Nitrous oxide (Drug)

结局指标

主要结局

Pain intensity

时间窗: 30 min of inhalation

Subjects underwent a 3 min cold immersion test at 30 min of inhalation and then provided response to pain intensity questionnaire

Psychomotor performance

时间窗: Baseline, 5 min of inhalation; 5, 30, 60 minutes recovery

Subjects underwent psychomotor testing at baseline, during inhalation, and during recovery post inhalation

Cognitive performance

时间窗: Baseline, every 5 min during inhalation, 5, 30, & 60 min during recovery

Subject underwent memory, sedation, visual analog, and drug effects testing

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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