Taiwan Associated Genetic and Nongenetic Small Vessel Disease
Recruiting now
Conditions studied: Cerebral Small Vessel Diseases, Cadasil, HTRA1-Related Autosomal Dominant Cerebral Angiopathy, COL4A1-Related Brain Small Vessel Disease With Haemorrhage, Fabry Disease, Magnetic Resonance Imaging, Next-generation Sequencing, Stroke
In brief
The TAG-SVD enrolled patients with clinical and neuroimaging features of cerebral small vessel disease (CSVD). All enrolled patients will receive next-generation sequence (NGS) with probes designed to target five candidate CSVD genes, and patients will be divided into genetic or non-genetic groups accordingly. Their clinical features and outcome will be followed for at least 2 years.
Key facts
- Study ID
- NCT05473637
- Run by
- National Taiwan University Hospital
- People needed
- 500
- Starts
- 2019-01-01
- Expected to finish
- 2028-12-31
- Last updated by the study team
- 2026-01-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Participants must have at least one of the following symptoms/signs or history
- stroke (especially small vessel occlusion type of ischaemic stroke, spontaneous ICH or young stroke)
- cognitive impairment or dementia
- gait disturbance
- parkinsonism (especially vascular parkinsonism features)
- headache (especially migraine)
- positive family history of hereditary CSVD
- MRI evidence of CSVD (MRI may be done for other reasons), including mild to moderate white matter hyper intensity, any lacune, or any cerebral microbleed
You may not qualify if…
- MRI evidence of CSVD due to other inflammatory, malignancy, or structural lesions
- patients or family members not willing to sign informed consent
Where it is running
- Department of Neurology, National Taiwan University Hospital — Taipei, Taiwan (enrolling)
Full record on ClinicalTrials.gov
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