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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000258
Other study ID # NIDA-08391-10
Secondary ID R01DA008391R01-0
Status Completed
Phase N/A
First received September 20, 1999
Last updated May 26, 2015
Start date April 1996
Est. completion date November 1997

Study information

Verified date May 2015
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date November 1997
Est. primary completion date November 1997
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 21 Years to 32 Years
Eligibility Please contact site for information.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator)


Intervention

Drug:
Nitrous oxide 10% & placebo

Nitrous oxide 20% & placebo

Nitrous oxide 30% & placebo

Nitrous oxide 40% and placebo


Locations

Country Name City State
United States University of Chicago, Anesthesia & Critical Care Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
University of Chicago National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

References & Publications (1)

Zacny JP, Cho AM, Toledano AY, Galinkin J, Coalson DW, Klock PA, Klafta JM, Young CJ. Effects of information on the reinforcing, subjective, and psychomotor effects of nitrous oxide in healthy volunteers. Drug Alcohol Depend. 1997 Nov 25;48(2):85-95. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Choice of nitrous oxide vs placebo 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. After 30 min inhalation of each No
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