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
40 participants
OBSERVATIONAL
2011-05-31
2012-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Propofol
Observation
There is no intervention, this is an observational study.
Interventions
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Observation
There is no intervention, this is an observational study.
Eligibility Criteria
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Inclusion Criteria
2. Routine (elective) surgical patients with ASA classifications of 1 or 2 (healthy).
3. Patients that are already scheduled to receive inhalational induction followed by IV propofol.
Exclusion Criteria
1 Year
ALL
No
Sponsors
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Nationwide Children's Hospital
OTHER
Responsible Party
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Christopher Lancaster
Attending Anesthesiologist
Principal Investigators
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Christopher Lancaster, MD
Role: PRINCIPAL_INVESTIGATOR
Nationwide Children's Hospital
Locations
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Nationwide Children's Hospital
Columbus, Ohio, United States
Countries
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Other Identifiers
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IRB11-00236
Identifier Type: -
Identifier Source: org_study_id
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