Actively Recruiting

Age: 40Years +
All Genders
ID05322824

Clinical Registration Study of Patients With Intracranial / Carotid Stenosis

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2023-04-18

500

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting data from patients aged 40 and older who have significant narrowing (stenosis) of the intracranial or carotid arteries to study how this condition relates to cognitive impairment. The study aims to analyze clinical information, brain imaging, and neuropsychological test results to identify early signs of cognitive decline in these patients. This is an observational registration study supported by the Second Affiliated Hospital, School of Medicine, Zhejiang University. Participants will receive standard medical treatment and may undergo interventional stenting as part of their care, though the study mainly observes and collects data without assigning specific treatments. Data collection includes clinical assessments and various brain imaging techniques. The study follows patients prospectively to monitor changes over time. During the study, participants will undergo cognitive testing using several scales such as the Mini-mental State Examination, Montreal Cognitive Assessment, Colour Trail Test, Hopkins Verbal Learning Test, clock drawing test, Animal Fluency Test, and Olfactory stick test. Researchers will also assess cerebral blood flow, glymphatic function, stroke incidence, and metabolic changes over a two-year follow-up period. Participants will be monitored regularly to track these outcomes and any safety concerns.

CONDITIONS

Brief Title

Clinical Registration Study of Patients With Intracranial / Carotid Stenosis

Who Can Participate

Age: 40Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 40 years or older
  • At least 50% stenosis in one side of the intracranial or carotid artery
  • Written informed consent provided
Not Eligible

You will not qualify if you...

  • Previous major head trauma or any brain surgery
  • Brain abnormalities such as hemorrhage or space-occupying lesions
  • Movement disorders or mental illness affecting cognitive testing
  • Severe loss of vision, hearing, or ability to communicate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 2 years

Participants are observed while receiving standard medical treatment or interventional stenting as part of their clinical care.

Regular visits to assess cognitive and neurological function over 2 years

Trial Site Locations

Total: 1 location

1

Second Affilated Hospital of Zhejiang University, School of Medicine

Hangzhou, Zhejiang, China, 310009

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Research Team

M

Min Lou, PhD, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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