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Effects of Subanesthetic Concentrations of Isoflurane/Nitrous Oxide - 3

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The University of Chicago

Status and phase

Completed
Phase 2

Conditions

Opioid-Related Disorders
Substance-Related Disorders

Treatments

Other: 100% oxygen
Drug: 0.4% isoflurane
Drug: 0.2% isoflurane
Drug: 30% N2O

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00000251
R01DA008391 (U.S. NIH Grant/Contract)
NIDA-08391-3
R01-08391-3

Details and patient eligibility

About

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 evaluate the acute and residual effects of subanesthetic concentrations of isoflurane/nitrous oxide combinations in healthy volunteers.

Enrollment

10 patients

Sex

All

Ages

21 to 32 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Please contact site for information.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

10 participants in 6 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
Subjects inhale 100% oxygen
Treatment:
Other: 100% oxygen
30% N2O
Active Comparator group
Description:
Subjects inhale 30% N2O
Treatment:
Drug: 30% N2O
0.2% isoflurane
Active Comparator group
Description:
Subjects inhale 0.2% isoflurane
Treatment:
Drug: 0.2% isoflurane
0.4% isoflurane
Active Comparator group
Description:
Subjects inhale 0.4% isoflurane
Treatment:
Drug: 0.4% isoflurane
0.2% isoflurane + 30% N2O
Active Comparator group
Description:
Subjects will inhale a combination of 0.2% isoflurane and 30% N2O
Treatment:
Drug: 0.2% isoflurane
Drug: 30% N2O
0.4% isoflurane + 30% N2O
Active Comparator group
Description:
Subjects will inhale a combination of 0.4% isoflurane and 30% N2O
Treatment:
Drug: 0.4% isoflurane
Drug: 30% N2O

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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