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Clinical Registration Study of Patients With Intracranial / Carotid Stenosis

Zhejiang University logo

Zhejiang University

Status

Enrolling

Conditions

Cognitive Function
Stenosis

Treatments

Procedure: Interventional stenting
Drug: standard medical treatment

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Through prospective registration and follow-up, this study will collect data of patients with intracranial/carotid stenosis, including clinical information, neuropsychological scales, multimodal magnetic resonance images. The investigators aim to analyze clinical and imaging characteristics of patients with cognitive impairment related to intracranial/carotid stenosis, in order to achieve early identification of cognitive impairment.

Enrollment

500 estimated patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged ≥ 40 years
  • ≥ 50% stenosis in unilateral intracranial / carotid artery
  • Written informed consent available

Exclusion criteria

  • Previous history of major head trauma and any intracranial surgery
  • Intracranial abnormalities, such as intracerebral hemorrhage, subarachnoid hemorrhage and other space occupying lesions
  • Extrapyramidal symptoms or mental illness which may affect neuropsychological measurement
  • Severe loss of vision, hearing, or communicative ability

Exit Criteria:

  • Not meet the inclusion criteria
  • For any poor adherence, not comply with the requirements of the follow-up, or safety reasons determined by investigator
  • Any adverse or serious adverse events during the study period judged by investigator

Trial contacts and locations

1

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Central trial contact

Min Lou, PhD, MD

Data sourced from clinicaltrials.gov

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