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Cerebral Small Vessel Disease Registry Study

Cerebral Small Vessel Disease Registry Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04318119
Enrollment
3000
Registered
2020-03-23
Start date
2019-11-18
Completion date
2055-11-18
Last updated
2023-09-28

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

Conditions

Cerebral Small Vessel Diseases

Brief summary

The aim of this study is to determine the clinical spectrum and natural progression of Cerebral Small Vessel Disease (CSVD) and in a prospective multicenter study, to assess the clinical, genetic and epigenetic features of patients with CSVD, , to find independent imaging markers, and to optimize clinical management.

Interventions

None listed

Sponsors

Bin Cai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

1. Sign informed consent. 2. Age\>18 3. At least one of the following CSVD MRI characteristics: ①recent small subcortical infarct;②lacune of presumed vascular origin;③white matter hypertensity of presumed vascular origin;④perivascular space;⑤cerebral microbleeds;⑥brain atrophy

Exclusion criteria

1. Unable to cooperate with inspectors 2. Non-vascular white matter lesions 3. Other cognitive diseases (such as alzheimer's disease, Parkinson's disease or thyroid disease) 4. Serious systemic illness, such as heart, liver, kidney disease or major mental illness 5. Contraindications for imaging examination

Design outcomes

Primary

MeasureTime frameDescription
Overall outcomes in patients with cerebral small vessel disease.From date of enrollment until the date of death from any cause, assessed up to 30 yearsrecord the occurrence of stroke and use modified Rankin Scale (mRS) to measure the degree of disability or dependence in the daily activities of people who have suffered a stroke or other causes of neurological disability.

Secondary

MeasureTime frameDescription
the development of lacunes in MRIFrom date of enrollment until the date of death from any cause, assessed up to 30 yearsrecord the number and location of lacunes
the development of the burden of microbleeds in MRIFrom date of enrollment until the date of death from any cause, assessed up to 30 yearsusing MARS scale to evaluate the development of the burden of microbleeds
the development of the burden of white matter hypertension in MRIFrom date of enrollment until the date of death from any cause, assessed up to 30 yearsusing Fazakes scale to evaluate the development of the burden of white matter hypertension
the development of enlarged perivascular space in MRIFrom date of enrollment until the date of death from any cause, assessed up to 30 yearsrecord the number and location of enlarged perivascular space

Countries

China

Contacts

Primary ContactBin Cai, PhD
caibin929@163.com13338413842

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026