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临床试验/NCT00000254
NCT00000254已完成2 期

Isoflurane at Subanesthetic Concentrations

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1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 response

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 test the hypothesis that isoflurane at subanesthetic concentrations does not reduce cold-water immersion pain 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 34 Years(Adult)
性别
Male
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% isoflurane

Sham Comparator

干预措施: 40% Nitrous oxide (Drug)

0% isoflurane

Sham Comparator

干预措施: Sham comparator (Other)

0.2% isoflurane

Active Comparator

干预措施: 40% Nitrous oxide (Drug)

0.2% isoflurane

Active Comparator

干预措施: 0.2% isoflurane (Drug)

0.4% isoflurane

Active Comparator

干预措施: 40% Nitrous oxide (Drug)

0.4% isoflurane

Active Comparator

干预措施: 0.4% isoflurane (Drug)

0.6% isoflurane

Active Comparator

干预措施: 40% Nitrous oxide (Drug)

0.6% isoflurane

Active Comparator

干预措施: 0.6% isoflurane (Drug)

结局指标

主要结局

Pain response

时间窗: Post inhalation

Effects of inhaled isoflurane on pain from immersion of subject's arm in ice cold water. Nitrous oxide (40%) was used as a positive control to confirm sensitivity of the pain assay.

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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