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The longitudinal MRI study for Alzheimer's disease and subcortical ischemic vascular dementia

The longitudinal MRI study for Alzheimer's disease and subcortical ischemic vascular dementia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027943
Enrollment
Unknown
Registered
2019-12-06
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Alzheimer's disease, vascular dementia

Interventions

Case series:Nil

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for AD: 1. Patients meet the diagnostic criteria of DSM-5 for major neurocognitive disorders and the diagnostic criteria of IWG-2 for AD, aged 50-85 years, and with an educational level of no less than 3 years; 2. Presence of an early and significant episodic memory impairment, gradual and progressive change in memory function reported by patient or informant over more than 6 months, objective evidence of anamnestic syndrome of the hippocampal type; CDR score = 1 to 2, MMSE score 10~26; 3. No evidence of significant cerebrovascular disease is shown on MRI, such as multiple cortical infarction or strategic infarction, lacune in basal ganglia area >1, and severe white matter hyperintensities (WMH); Fazekas score 3 months; absence of dementia; MMSE score > 24, CDR score = 0.5; 3. No evidence of significant cerebrovascular disease is shown on MRI, such as multiple cortical infarction or strategic infarction, lacune in basal ganglia area >1, and severe white matter hyperintensities (WMH); Fazekas score =3) supratentorial subcortical lacunes (3–15 mm in diameter), with/without WMH; (2) moderate to severe WMH according to the Fazekas rating scale >= 2 with/without lacunes; (3) one or more lacunar infarcts outside the brainstem, strategically placed in the subcortical deep grey matter. Inclusion criteria for healthy control: 1. Absence of subjective memory complaints, and performance within the normal range on neuropsychological measures; age range 50-85 years, with an educational level of no less than 3 years; 2. CDR score = 0, MMSE score > 26; 3. No clinically significant atrophy in the medial temporal lobe or other brain areas on MRI, no extensive WMH, Fazekas score < 2.

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment caused by other central nervous system diseases, such as frontotemporal lobe degeneration, dementia with Lewy bodies, Parkinson's disease dementia, multiple sclerosis and hydrocephalus; 2. Cognitive impairment caused by other medical conditions, such as thyroid dysfunction, vitamin B12 deficiency, syphilis or HIV infection; 3. Medication for cogntive impairment or cerebrovascular disease is adjusted within 4 weeks before baseline; 4. A history of drug or alcohol abuse; 5. Severe visual or auditory disability that could influence performance on cognitive assessments.

Design outcomes

Primary

MeasureTime frame
cerebral blood flow;brain volume;brain function;the integrity of white matter;

Secondary

MeasureTime frame
AVLT;BVMT-R;SDMT;TMT-A/B;BNT;COWAT;DS;SCWT;Verbal fluency test;MMSE;ADL;CDR;NPI;CDU;TCD;

Countries

China

Contacts

Public ContactNan Zhang

Tianjin Medical University General Hospital

nanzhang@tmu.edu.cn+86 13752128310

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026