Sevoflurane vs Nitrous Oxide Inhalation at Subanesthetic Concentrations - 11
NCT ID: NCT00000259
Last Updated: 2015-05-28
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
NA
12 participants
INTERVENTIONAL
1996-08-31
1997-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
CROSSOVER
DOUBLE
Study Groups
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Placebo
Subject inhales no drug (100% oxygen)
Placebo
0.3% sevoflurane
0.3 % Sevoflurane
0.6% sevoflurane
0.6% Sevoflurane
15% Nitrous oxide
15 % Nitrous oxide
30% Nitrous oxide
30% Nitrous oxide
Interventions
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15 % Nitrous oxide
0.3 % Sevoflurane
30% Nitrous oxide
0.6% Sevoflurane
Placebo
Eligibility Criteria
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Inclusion Criteria
21 Years
39 Years
ALL
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. 1997 (in press).
Other Identifiers
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R01-08391-11
Identifier Type: -
Identifier Source: secondary_id
NIDA-08391-11
Identifier Type: -
Identifier Source: org_study_id
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