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
855 participants
OBSERVATIONAL
2015-10-31
2016-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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DEX
patients who received dexmedetomidine during the operation
Dexmedetomidine
PPF
patients who received propofol during the operation
Propofol
Interventions
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Dexmedetomidine
Propofol
Eligibility Criteria
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Inclusion Criteria
* age of 65 years or greater
Exclusion Criteria
* age \< 65 years
* central nervous system disease, including dementia and Parkinson's disease
* Patients who were not received sedation with propofol or dexmedetomidine during the operation
65 Years
ALL
No
Sponsors
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Seoul National University Bundang Hospital
OTHER
Responsible Party
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Hyo-Seok Na
Associate Professor
Locations
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Seoul National University Bundang Hospital
Seongnam-si, Gyeonggi-do, South Korea
Countries
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Other Identifiers
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B-1510/318-104
Identifier Type: -
Identifier Source: org_study_id
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