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Registry study of white matter hyperintensity without overt traditional risk factors

Registry study of white matter hyperintensity without overt traditional risk factors

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100043995
Enrollment
Unknown
Registered
2021-03-06
Start date
2021-04-27
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

cerebral small vessel disease

Interventions

case series:Nil

Sponsors

Beijing Tiantan Hospital affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18 - 60 years. 2) Presence of white matter hyperintensity on MRI (except for PVH Fazekas score=1 only). 3) Without hypertension (hypertension was defined as systolic blood pressure (SBP) >= 140 mmHg or diastolic blood pressure (DBP) >= 90 mmHg at admission, or having a history of hypertension or receiving antihypertensive therapy). 4) Without diabetes (diabetes was defined as patients with level of fasting plasma glucose (FPG) >= 7.0 mmol/L or 2 hour postprandial blood glucose (2hPBG)>= 11.1mmol/L or random plasma glucose (RPG) >= 11.1mmol/L or glycated hemoglobin A1c (HbA1c) concentration >= 6.5% or having a history of diabetes or receiving glucose-lowering drugs or insulin). 5) With non-traditional risk factors (with more than 1 of the following characteristics: hypotension, migraine, sleep disorders, fatigue, anxiety, chronic psychological stress, social relations disorders). 6) Independent in activities of daily life (modified Rankin Scale (mRS) <= 2). 7) Provide written informed consent.

Exclusion criteria

Exclusion criteria: 1) History of stroke, including cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage. 2) Acute cerebral infarction with the lesion showing high signal on DWI phase and the diameter > 20mm; acute subarachnoid hemorrhage or previous history of cerebrovascular malformation, aneurysmal subarachnoid hemorrhage or untreated aneurysms (> 3mm in diameter). 3) Drugs that affect autonomic nervous functions, such as adrenergic receptors and cholinesterase receptors, are being taken. 4) Diagnosed center neurodegenerative diseases (e.g. AD, PD, dementia). 5) Diagnosed autonomic nervous dysfunction diseases, such as Raynaud's disease. 6) Hereditary cerebrovascular diseases that have been diagnosed or known. 7) Presence of non-vascular white matter lesions, for example, multiple sclerosis, adult white matter dysplasia, metabolic encephalopathy or anoxic brain injury. 8) Autoimmune diseases, such as lupus erythematosus, rheumatoid arthritis. 9) Severe organic disease, such as malignant tumor, with a life expectancy less than 5 years. 10) Participate in other clinical trials at the same time.

Design outcomes

Primary

MeasureTime frame
Imaging features of white matter hyperintensity;Imaging progression of white matter hyperintensity within 5 years;Clinical symptoms of the subjects;Progress of clinical characteristics of subjects within 5 years;Autonomic nervous function;

Countries

China

Contacts

Public ContactYilong Wang

Beijing Tiantan Hospital affiliated to Capital Medical University

yilongwang528@163.com+86 13911666571

Outcome results

None listed

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