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Clinical Trials/KCT0005428
KCT0005428
Recruiting
未知

Building vascular cognitive impairment cohort for development of a dementia risk assessment system and identification of pathophysiologycal interaction between vascular aging and neurodegeneration.

Gachon University Gil Medical Center0 sites360 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Gachon University Gil Medical Center
Enrollment
360
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Cognitively Normal (CN)
  • Normal cognition will be defined according to neuropsychological testing, which didn't fall within 1\.5 SD, and Clinical Dementia Rating (CDR) was 0 .
  • \- Mild cognitive impairment (MCI):
  • CDR was 0\.5
  • Subjects were not be clinically diagnosed with dementia according to Diagnostic and Statistical Manual of Mental Disorders, 4th. Edition, Text\-revision (DSM\-IV\-TR) criteria.
  • \- Dementia (AD and SVaD)
  • \- Alzheimer's disease (AD)
  • CDR \= 0\.5
  • subjects were diagnosed with dementia according to DSM\-IV\-TR.
  • subjects were diagnosed with probable AD or possible AD according to the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer’s Disease and Related Disorders Association (NINCDS\-ADRDA) criteria.

Exclusion Criteria

  • \- Subjects who do not meet the inclusion criteria.
  • \- Subjects who have history of any significant neurological disease other than AD or VD , such as traumatic brain injury, Parkinson's disease, Huntington's disease, motor neuron disease, or multiple sclerosis.
  • \- Subjects who have history of brain tumor, normal presure hydrocephalus, encephalitis, or metabolic encephalopathy.
  • \- Subjects who have history of a massive stroke in cerebrum, brain strem or cerebellum.
  • \- Subjects who have history of psychiatric disorder.
  • \- Subjects unable to undergo MRI or PET scanning.
  • \- Pregnent or reast feeding women.

Outcomes

Primary Outcomes

Not specified

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