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临床试验/NCT00000255
NCT00000255已完成2 期

Differential Acute Tolerance Development to Effects of 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: 1995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
Pain intensity, pain bothersomeness

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 examine differential acute tolerance development to effects of nitrous oxide 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, Investigator)

入排标准

年龄范围
21 Years 至 37 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

30% nitrous oxide

Active Comparator

干预措施: Nitrous oxide (Drug)

20% nitrous oxide

Active Comparator

干预措施: Nitrous oxide (Drug)

0% Nitrous oxide

Placebo Comparator

干预措施: Nitrous oxide (Drug)

10% nitrous oxide

Active Comparator

干预措施: Nitrous oxide (Drug)

40% nitrous oxide

Active Comparator

干预措施: Nitrous oxide (Drug)

结局指标

主要结局

Pain intensity, pain bothersomeness

时间窗: 25, 70, & 115 min of inhalation and 40 min post

Subjects will inhale varying conc of nitrous oxide for 120 min with cold immersion of forearm at 25, 70, and 115 min and 40 min after inhalation. Pain intensity and bothersomeness will be assessed at each immersion.

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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