Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy
MONDO:0007432Also known as: CADASIL, cerebral arteriopathy with subcortical infaracts and leukoencephalopathy, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, Casil, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, dementia, hereditary multi-infarct type
17 clinical trials for this condition and its sub-types.
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Broader categories
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Could a palm extract help fight a rare genetic brain disease?
Disease control CompletedThis study tested a supplement called HOV-12020 (made from palm tocotrienols) in 50 adults aged 45-75 with CADASIL, a rare genetic disease that damages small blood vessels in the brain, leading to strokes and memory loss. The goal was to see if the supplement could reduce worseni…
Phase: PHASE2 • Sponsor: Hovid Berhad • Aim: Disease control
Last updated Jun 27, 2026 09:02 UTC
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NIH launches study to unravel mysteries of rare genetic brain disease CADASIL
Knowledge-focused CompletedThis study looked at 20 people with CADASIL, a rare genetic disease that damages brain arteries and causes migraines, strokes, and dementia. Researchers used blood tests, skin biopsies, eye exams, and brain scans to learn more about how the disease works. The goal was to better u…
Sponsor: National Heart, Lung, and Blood Institute (NHLBI) • Aim: Knowledge-focused
Last updated Aug 15, 2026 00:00 UTC
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Brain scans reveal hidden clues in rare stroke disorder
Knowledge-focused CompletedThis study looked at how blood flow and brain activity are linked in people with CADASIL, a rare genetic disease that causes small strokes. Researchers used MRI and EEG scans to measure these connections in 60 adults. The goal was to better understand the disease, not to test a n…
Sponsor: Institut National de la Santé Et de la Recherche Médicale, France • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:11 UTC
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Could a single DNA test solve the mystery of rare brain diseases in kids?
Knowledge-focused CompletedThis study looked at whether whole genome sequencing (a complete read of a person's DNA) can help diagnose leukodystrophies, a group of rare brain diseases that are hard to identify. Researchers enrolled 236 children with white matter abnormalities on brain scans but no known gen…
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:56 UTC