Skip to content

Neuroimaging Correlates of Memory Decline Following Carotid Interventions

Neuroimaging Correlates of Memory Decline Following Carotid Interventions

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02006095
Enrollment
207
Registered
2013-12-09
Start date
2012-11-30
Completion date
2018-04-30
Last updated
2022-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carotid Artery Stenosis

Keywords

carotid artery stenting, carotid endarterectomy, magnetic resonance imaging (MRI), neuropsychological testing, microemboli

Brief summary

Carotid revascularization can significantly reduce the risk of stroke in patients with severe carotid stenosis; however, it has been associated with cognitive decline in 25% of the older adults who undergo the procedure. Characterizing risk factors for cognitive decline following carotid interventions and individualizing treatment strategy based on those risks can minimize procedure-associated cognitive dysfunction. Neuroimaging techniques that characterize white matter integrity and regional hypoperfusion have the potential to provide sensitive brain structure indicators that may be associated with memory decline following revascularization procedures. In this protocol, we hope to determine how cerebral blood flow and baseline white matter abnormality in the vulnerable region modify the frequency and cognitive effect of microembolization following carotid revascularization procedures.

Interventions

OTHERMagnetic resonance imaging

arterial spin labeling, diffusion tensor imaging, and diffusion weighted imaging sequences will be used

BEHAVIORALNeuropsychological testing

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patient is male or female \>40 yrs of age. * Patient has occlusive extracranial carotid stenosis (≥70%) * Patient is scheduled to undergo a carotid revascularization procedure * Patient agrees to voluntarily participate in the study and signs an informed consent. * Patient agrees to be available for follow-up and is able to participate in all study testing procedures. * Patient has sufficient visual and auditory acuity for cognitive testing.

Exclusion criteria

* Patient is unable to safely and comfortably undergo MR imaging procedures (e.g., claustrophobia, implanted medical devices that are MRI incompatible such as pacemaker, defibrillator, neural stimulator etc) * Patient has an untreated or unsuccessfully controlled psychiatric disease (schizophrenia, bipolar disorder). * Patient has prominent suicidal or homicidal ideation. * Patient has acute illness or unstable chronic illness (e.g. uncontrolled hypertension, hepatic encephalopathy, portal hypertension, ascites, and esophageal varices, pancreatitis). * Patient with a history of neurological (e.g., multiple sclerosis, seizure disorder, Parkinson's disease) or systemic illness affecting central nervous system function. * Patient has prior closed head injury with ≥24 hours of amnesia.

Design outcomes

Primary

MeasureTime frameDescription
Brain MRI scans6 months following the procedureWhite matter abnormality and perfusion in correlation with microembolization and cognitive change

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026