Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
10 participants
INTERVENTIONAL
1995-01-31
1995-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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0% isoflurane
40% Nitrous oxide
Used as pain assay positive control
Sham comparator
0% isoflurane in oxygen
0.2% isoflurane
40% Nitrous oxide
Used as pain assay positive control
0.2% isoflurane
0.4% isoflurane
40% Nitrous oxide
Used as pain assay positive control
0.4% isoflurane
0.6% isoflurane
40% Nitrous oxide
Used as pain assay positive control
0.6% isoflurane
Interventions
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40% Nitrous oxide
Used as pain assay positive control
Sham comparator
0% isoflurane in oxygen
0.2% isoflurane
0.4% isoflurane
0.6% isoflurane
Eligibility Criteria
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Inclusion Criteria
21 Years
34 Years
MALE
Yes
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
University of Chicago
OTHER
Responsible Party
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Principal Investigators
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James Zacny, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Chicago
Locations
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University of Chicago, Anesthesia & Critical Care
Chicago, Illinois, United States
Countries
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References
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Anesthesiology, 1995, 83: A287
Other Identifiers
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R01-08391-6
Identifier Type: -
Identifier Source: secondary_id
NIDA-08391-6
Identifier Type: -
Identifier Source: org_study_id
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