Neurocognitive Dysfunction After Anesthesia in Patients With Recent Concussion
NCT ID: NCT03952208
Last Updated: 2025-04-16
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
52 participants
INTERVENTIONAL
2019-02-21
2025-04-10
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
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Concussion Group
Subjects diagnosed with concussion defined as a clinician-diagnosed disease by the International Classification of Diseases (ICD)-10 due to a head injury with a Glasgow Coma Score ≥13 undergoing a planned surgery/anesthetic standard of care will undergo neurocognitive testing pre and post surgery/anesthetic.
Neurocognitive Testing
A comprehensive assessment of neuropsychometric measures to evaluate cognitive functioning.
Matched Subjects Group
Matched subjects without concussion undergoing a planned surgery/anesthetic standard of care, matching for procedural type, sex, age ± 2 years, and adherence to the exclusion criteria will undergo neurocognitive testing pre and post surgery/anesthetic.
Neurocognitive Testing
A comprehensive assessment of neuropsychometric measures to evaluate cognitive functioning.
Interventions
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Neurocognitive Testing
A comprehensive assessment of neuropsychometric measures to evaluate cognitive functioning.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
16 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Arnoley (Arney) S. Abcejo
Principal Investigator
Principal Investigators
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Arnoley S Abcejo, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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18-006578
Identifier Type: -
Identifier Source: org_study_id
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