Assessing Neurocognition After Cerebrovascular Intervention
NCT03344276 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2025-02-06
Summary
Decreased blood flow to the brain can cause decreased cognitive function. Carotid disease can result in decreased blood flow to the brain. The investigators seek to assess this relationship prospectively through performing a battery of neurocognitive assessments, collection of serum markers of inflammation, and through neuroimaging at two points before intervention (2 months and 1 month before stenting) and at two points after intervention (1 month and 2 months after intervention). The goal is to provide prospective evidence to identify the extent to which carotid stenosis and hypoperfusion of the brain results in diminished neurocognitive performance, and see if serum biomarkers before and after stenting correlate with these findings.
Conditions
- Carotid Artery Diseases
- Neurocognitive Dysfunction
Interventions
- DIAGNOSTIC_TEST
-
Neurocognitive Assessments
Patients will undergo carotid artery stenting for 50-70% carotid artery stenosis. Prior to surgery patients will undergo a battery of neurocogntive assessments 1 month and 2 months prior to surgery.
- DIAGNOSTIC_TEST
-
Measurements of inflammatory biomarkers
Patients will undergo carotid artery stenting for 50-70% carotid artery stenosis. After surgery, patients will undergo blood draws to measure for inflammatory biomarkers.
- PROCEDURE
-
Carotid Artery Stenting
Patients will undergo carotid artery stenting for 50-70% carotid artery stenosis.
Sponsors & Collaborators
-
University of California, San Diego
lead OTHER
Principal Investigators
-
Alexander A Khalessi, MD · UC San Diego
-
David R Santiago-Dieppa, MD · UC San Diego
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-07-15
- Primary Completion
- 2025-10-31
- Completion
- 2025-12-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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