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Clinical Trials/NCT00000258
NCT00000258
Completed
Not Applicable

Role of Instructions in Nitrous Oxide Effects and Choice

University of Chicago1 site in 1 country22 target enrollmentApril 1996

Overview

Phase
Not Applicable
Intervention
Nitrous oxide 10% & placebo
Conditions
Opioid-Related Disorders
Sponsor
University of Chicago
Enrollment
22
Locations
1
Primary Endpoint
Choice of nitrous oxide vs placebo
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

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 evaluate the role of instructions in nitrous oxide subjective effects and choice.

Registry
clinicaltrials.gov
Start Date
April 1996
End Date
November 1997
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Informed group

Group inhaled placebo and varying doses of nitrous oxide in pairs then chose which they wanted for a third inhalation.

Intervention: Nitrous oxide 10% & placebo

Informed group

Group inhaled placebo and varying doses of nitrous oxide in pairs then chose which they wanted for a third inhalation.

Intervention: Nitrous oxide 20% & placebo

Informed group

Group inhaled placebo and varying doses of nitrous oxide in pairs then chose which they wanted for a third inhalation.

Intervention: Nitrous oxide 30% & placebo

Informed group

Group inhaled placebo and varying doses of nitrous oxide in pairs then chose which they wanted for a third inhalation.

Intervention: Nitrous oxide 40% and placebo

Non-informed Group

Group and technician were blinded as to which gas they were inhaling in pairs with third inhalation subject's choice.

Intervention: Nitrous oxide 10% & placebo

Non-informed Group

Group and technician were blinded as to which gas they were inhaling in pairs with third inhalation subject's choice.

Intervention: Nitrous oxide 20% & placebo

Non-informed Group

Group and technician were blinded as to which gas they were inhaling in pairs with third inhalation subject's choice.

Intervention: Nitrous oxide 30% & placebo

Non-informed Group

Group and technician were blinded as to which gas they were inhaling in pairs with third inhalation subject's choice.

Intervention: Nitrous oxide 40% and placebo

Outcomes

Primary Outcomes

Choice of nitrous oxide vs placebo

Time Frame: After 30 min inhalation of each

Subjects inhaled placebo and varying per centages of nitrous oxide in sampling pair, then chose for third inhalation. One group was told which of the gases they were inhaling during sampling and one group as well as the technician administering the inhalant was blinded. Psychomotor tests were done at each dose.

Study Sites (1)

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