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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000263
Other study ID # NIDA-08391-15
Secondary ID R01DA008391R01-0
Status Completed
Phase N/A
First received September 20, 1999
Last updated May 26, 2015
Start date January 1997
Est. completion date October 1998

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 determine the effects of combined alcohol and nitrous oxide intake on mood, psychomotor performance, and the pain response in healthy volunteers.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date October 1998
Est. primary completion date October 1998
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Please contact site for information.

Study Design

Allocation: Non-Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver)


Intervention

Drug:
30% Nitrous oxide

Other:
0.25 g/Kg ethanol

0.5 g/KG ethanol

0 g/Kg ethanol


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, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain intensity, pain bothersomeness Post inhalation No
Primary Mood Post inhalation No
Primary Psychomotor performance Post inhalation No
Primary Cognitive performance Post inhalation No
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