Assessing cognitive function after carotid artery stenting
Official title: Assessing Neurocognition After Cerebrovascular Intervention
Run by University of California, San Diego · NCT03344276 · Data updated 2026-11-12
This study is testing how carotid artery stenting affects thinking and memory in people with narrowed carotid arteries by checking their cognitive skills and brain blood flow before and after the procedure.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | University of California, San Diego Academic / other |
| Locations | 1 site (San Diego, California) |
| Status | Recruiting |
| Started | July 15, 2021 |
| Main results expected | October 2025 |
| Study ends | December 2025 |
| Registry record updated | February 6, 2025 |
| Trial ID | NCT03344276 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults over 18 with either symptomatic carotid stenosis of 50% or greater or asymptomatic stenosis of 70% or greater.
✕Probably not a fit
Patients requiring emergency carotid stenting or those with acute symptoms may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate the relationship between carotid artery disease and neurocognitive dysfunction by conducting a series of cognitive assessments and collecting serum markers of inflammation before and after carotid artery stenting. Patients with significant carotid stenosis will undergo cognitive testing at two points prior to the intervention and two points following it, allowing researchers to analyze changes in cognitive performance. Additionally, neuroimaging will be performed to assess brain blood flow and its correlation with cognitive outcomes. The study seeks to provide prospective evidence on how carotid stenosis impacts cognitive function and the potential role of inflammatory markers.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of cognitive dysfunction in patients with carotid artery disease.
How similar studies have gone: While there have been studies on carotid artery disease and cognitive function, this specific approach of using within-subjects design and serum biomarkers is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients \>18 years of age * ultrasound evidence of carotid stenosis; in which the patient has either 50% or greater symptomatic carotid stenosis or 70% or greater asymptomatic carotid stenosis. Exclusion Criteria: 1. patients \<18 years of age 2. patients with without compatibility for MRI 3. patients requiring carotid stenting for reasons not related to long-standing stenosis 4. patients requiring emergency carotid stenting for acute symptoms such as crescendo transient ischemic attacks, intolerance of physiologic blood pressure. 5. Patients that do not have appropriate capacity (i.e. understand the risks and benefits associated with this study) or are unable to consent for themselves will not be included in this study.
Where it's running
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UCSD Medical Center
San Diego, California, United States Recruiting
Study contacts
- Principal investigator: Alexander A Khalessi, MD — UC San Diego
- Study coordinator: Alexander Khalessi, MD
- Email: akhalessi@ucsd.edu
- Phone: (619) 543-5540
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.