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Clinical Trials/ITMCTR1900002341
ITMCTR1900002341
Not yet recruiting
Phase 1

Clinical study for diagnostic markers in cerebrospinal fluid of Alzheimer's disease

The Third Affiliated Hospital of Zhejiang Chinese Medical University0 sitesTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Alzheimer's disease
Sponsor
The Third Affiliated Hospital of Zhejiang Chinese Medical University
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Diagnostic test
Sex
All

Investigators

Sponsor
The Third Affiliated Hospital of Zhejiang Chinese Medical University

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged\>\=60 years old;
  • 2\. Meet the diagnostic criteria of clinical typical AD;
  • 3\. Specific clinical phenotype, early and significant episodic memory impairment (isolated or other cognitive, behavioral changes associated with implicated dementia syndrome or mild cognitive impairment), including the following characteristics:
  • (1\) The patient or the insider complains that the memory ability has gradually declined over 6 months;
  • (2\) The objective evidence of the hippocampus type amnesia syndrome, based on the AD\-specific detection method\-\-through the clue recall test, found that the episodic memory ability decreased significantly, according to the simple intelligent mental state checklist MMSE diagnostic criteria: illiterate group \= 17 points, primary school group \= 20 points, middle school or above group \= 24 points (heavy disease in moderate stage dementia stage hippocampus amnesia syndrome may be difficult to identify, in vivo AD pathological evidence is sufficient to exist in the characteristics of dementia syndrome: cerebrospinal fluid Aß42 reduction, bilateral frontal apical area glucose radioactivity Counting drops significantly).

Exclusion Criteria

  • 1\. Severe hemodynamic instability and unstable vital signs;
  • 2\. Malignant arrhythmia, severe failure of organ function such as heart, lung, liver and kidney, suffering from tumor;
  • 3\. Cognitive impairment cannot be matched with lumbar puncture;
  • 4\. Participated in other clinical studies within 2 months prior to the start of the study;
  • 5\. The patient or his licensor is unwilling to sign a written informed consent or is unwilling to follow the research protocol;
  • 6\. Other types of dementia:
  • (1\) sudden onset;
  • (2\) Early symptoms: gait disorder, epilepsy, behavioral changes.
  • Clinical features:
  • (1\) focal neurological features;

Outcomes

Primary Outcomes

Not specified

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