Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
NCT07353502

miR-342-5p/AnkG Pathway in Early AD Synaptic Dysfunction

Led by The Fourth Affiliated Hospital of Zhejiang University School of Medicine · Updated on 2026-01-20

40

Participants Needed

1

Research Sites

37 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Alzheimer's disease is the most common memory loss disease among the elderly. This disease affects the patient's memory, language, attention, and behavioral abilities. Current research has found that in the early stages of the disease, synaptic connections between brain nerve cells become abnormal, but the specific cause is still unclear. Investigators' previous research discovered that in the brains of diseased mice, certain special substances (the miR 342 5p/AnkG-mediated pathway) might be related to this abnormality, and these substances can be detected in both blood and cerebrospinal fluid. Therefore, investigators want to further explore the specific mechanisms of abnormal nerve cell connections, seek biomarkers for early detection of the disease, and provide new ideas for early diagnosis in the future.

CONDITIONS

Official Title

miR-342-5p/AnkG Pathway in Early AD Synaptic Dysfunction

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • For Alzheimer's group: diagnosed with probable Alzheimer's dementia by NINCDS-ADRDA criteria
  • MMSE score between 0 and 23 points
  • Clinical Dementia Rating score of 0.5 or higher
  • Hachinski Ischemic Score less than 4 points
  • Brain MRI shows bilateral temporal lobe and hippocampal atrophy
  • Age 50 years or older
  • For control group: healthy individuals matched in age to Alzheimer's group
  • Normal cognitive function and good daily living activities
  • No dementia in first-degree relatives
  • Negative brain MRI and neurological exam
Not Eligible

You will not qualify if you...

  • Dementia or cognitive impairment caused by other diseases
  • History of substance abuse
  • Progressive primary aphasia
  • Previous traumatic brain injury
  • Comorbid depression, schizophrenia, or severe cardiovascular, liver, kidney, or blood diseases
  • Impaired consciousness or inability to cooperate
  • Other conditions unsuitable for inclusion

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Fourth Affiliated Hospital of Zhejiang University School of Medicine

Yiwu, Zhejiang, China, 322000

Actively Recruiting

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Research Team

X

Xu-hua Xu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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