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Cohort study of inpatient and outpatient patients with cerebral small vascular disease

Cohort study of inpatient and outpatient patients with cerebral small vascular disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071826
Enrollment
Unknown
Registered
2023-05-25
Start date
2023-05-11
Completion date
Unknown
Last updated
2023-06-12

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

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Participants aged between 18 and 80 years, with no restriction on gender. 2.Participants who have completed a 3.0T MRI of the head within one year at Yueyang Hospital, and meet the imaging diagnostic criteria of the 2013 STRIVE guidelines. 3.Participants who have a Modified Rankin Scale (mRS) score of 0-2 (able to perform activities of daily living) at the time of the visit. 4.Participants who are able to understand and agree to participate in the study, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Diagnosis of symptomatic lacunar syndrome without 6 months of onset (participants can be enrolled after 6 months to avoid the impact of the acute phase). 2.Intracranial and extracranial vascular examination confirms stenosis of the blood vessel by =50%. 3.Imaging data reveals intracranial space-occupying lesions. 4.A history of other neurological or mental illnesses with a definite diagnosis of the cause, including stroke (excluding lacunar infarctions), neurodegenerative diseases (such as Parkinson’s disease and Alzheimer’s disease). 5.Co-occurring serious illnesses, such as malignant tumors, heart failure, respiratory failure, renal failure, severe liver dysfunction, severe blood system diseases, or gastrointestinal bleeding. 6.Severe impairment in vision, hearing, language function, or limb muscular weakness that prevents completion of relevant tests. 7.Women who are pregnant or breastfeeding. 8.MRI scan contraindicated due to various reasons (such as claustrophobia). 9.Any other reasons that prevent the collection of clinical data required for this study.

Design outcomes

Primary

MeasureTime frame
Blood pressure variability;Imaging data;Neuro-psychological scale;

Secondary

MeasureTime frame
Demographic data;

Countries

China

Contacts

Public ContactYan Han

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

hanyan.2006@aliyun.com+86 189 1751 0069

Outcome results

None listed

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