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Application of MES scale, plasma Aß42, AGEs, fMRI low-frequency amplitude in the early diagnosis of Alzheimer's disease and early treatment of AD with electroencephalogram electrical stimulation

Application of MES scale, biomarkers and electroencephalogram electrical stimulation in the diagnosis and treatment of early Alzheimer's disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011965
Enrollment
Unknown
Registered
2017-07-13
Start date
2014-12-18
Completion date
Unknown
Last updated
2017-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's disease

Interventions

Mild-1 group:placebo
Mild-2 Group:FNS medication
MCI-1 Group:FNS medication
MCI-2 Group:Placebo

Sponsors

the Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. the normal control group(NC): using clinical dementia rating scale (CDR) to measure subjects' memory, direction, judgment and problem solving skills, social affairs, family life, hobbies, CDR =0. MCI group(MCI): using CDR to measure subjects' memory, direction, judgment and problem solving skills, social affairs, family life, hobbies, CDR= 0.5. The mild dementia group (mild AD): using CDR to measure subjects' memory, direction, judgment and problem solving skills, social affairs, family life hobbies CDR= 1.

Exclusion criteria

Exclusion criteria: 1. Severe vision or/and hearing impairment, can not complete cognitive function tests; 2. Anxiety, depression, severe insomnia recently; 3. cognitive dysfunction caused by Lack of folate, vitamin B12, thyroid disease, severe cardiopulmonary, liver, kidney, and other diseases of the nervous system?diseases (Lewy body dementiaCorticobasal ganglion degenerationHuntington's choreaProgressive supranuclear palsy; 4. Alcohol or drug dependence, a history of severe head injury; 5. past medical history of cerebrovascular disease (such as ischemic cerebral apoplexy, cerebral hemorrhage, moderate or severe leukoaraisosis, etc.); 6. Intracranial infection, viral encephalitis, CJD, AIDS, neurosyphilis); 7. Individuals with metal dentures,, bracket and other metal objects; 8. The subjects refused to participate the trial.

Design outcomes

Primary

MeasureTime frame
Cognitive scales;blood Aß42 and AGEs;BOLD-fMRI, ALFF;

Countries

China

Contacts

Public ContactXiaofeng LI

the Second Affiliated Hospital of Chongqing Medical University

lixfcq@qq.com+86 13032327639

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026