Completed

Effects of Behavioral Contingencies on Effects of Nitrous Oxide - 12

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Nitrous oxide

Drug
Who is being recruted

Opioid-Related Disorders

+ Substance-Related Disorders
Over 21 Years
How is the trial designed

Other Study

Interventional
Study Start: June 1997

Summary

Principal SponsorUniversity of Chicago
Last updated: May 27, 2015
Sourced from a government-validated database.Claim as a partner
Study start date: June 1, 1997Actual date on which the first participant was enrolled.

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 the effects of different behavioral contingencies in modulating the reinforcing effects of nitrous oxide in healthy volunteers.

Official TitleEffects of Behavioral Contingencies on Effects of Nitrous Oxide 
Principal SponsorUniversity of Chicago
Last updated: May 27, 2015
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details
18 patients to be enrolledTotal number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria
Any sexBiological sex of participants that are eligible to enroll.
Over 21 YearsRange of ages for which participants are eligible to join.
Healthy volunteers allowedIf individuals who are healthy and do not have the condition being studied can participate.
Conditions
Pathology
Opioid-Related Disorders
Substance-Related Disorders
Criteria
No eligibility criteria are available at this time.Please check with the study contact for more details. 
Anonymus Profile Image
Ensure optimum compatibilityAdd your profile to know your probability eligibility score.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives
Study Objectives
Primary Objectives


Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has 1 location
Suspended
University of Chicago, Anesthesia & Critical CareChicago, United StatesSee the location

CompletedOne Study Center