Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
MONDO:0000914A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.
Also known as: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, CADASIL, CADASIL syndrome, CADASIL type 1, CADASIL1, CASIL, autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1, cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1
17 clinical trials for this condition and its sub-types.
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The eyes may hold a window to brain health: a trial tests a new marker and treatment
Disease control Recruiting nowThis study investigates whether changes in retinal blood vessels can serve as a marker for cerebral small vessel disease (SVD), a common condition in older adults that increases stroke and dementia risk. The trial includes people with SVD-related conditions like CADASIL, sporadic…
Phase: PHASE1, PHASE2 • Sponsor: Mayo Clinic • Aim: Disease control
Last updated Aug 05, 2026 00:00 UTC
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Could your own stem cells heal your brain? new trial tests it
Disease control Recruiting nowThis study is testing whether stem cells taken from a person's own bone marrow and then given back through the veins and nose can improve brain and nerve function. It includes 500 people with various conditions like stroke, Parkinson's, Alzheimer's, and nerve damage. The goal is …
Phase: NA • Sponsor: MD Stem Cells • Aim: Disease control
Last updated Jun 28, 2026 00:00 UTC
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Scientists launch Decade-Long quest to unravel rare stroke disorder
Knowledge-focused Recruiting nowThis study follows 155 adults with CADASIL, a genetic condition that narrows small blood vessels and raises the risk of strokes and dementia, over nine years. Researchers will use brain scans, blood tests, and other exams to track how the disease changes blood vessels and thinkin…
Sponsor: National Heart, Lung, and Blood Institute (NHLBI) • Aim: Knowledge-focused
Last updated Aug 05, 2026 00:00 UTC
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10-Year study to track rare brain disease in 500 koreans
Knowledge-focused Recruiting nowThis 10-year study will follow 500 Korean adults with CADASIL, a genetic brain disease that causes strokes and dementia. Researchers will track symptoms, brain scans, memory tests, and genetic information to understand how the disease progresses in Koreans. The goal is to improve…
Sponsor: Jeju National University Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:33 UTC
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Rare stroke causes no longer overlooked: new italian network aims to diagnose and understand mysterious brain diseases
Knowledge-focused Recruiting nowThis study is creating a large network of hospitals across Italy to improve the diagnosis and understanding of rare cerebrovascular diseases (rCVDs), such as CADASIL, Fabry disease, and Moyamoya. Researchers will collect medical information and blood samples from 500 patients to …
Sponsor: Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:08 UTC
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Heart hole and migraine mystery: new study digs into genetic clues
Knowledge-focused Recruiting nowThis study is investigating why some people with migraine with aura also have a small hole in the heart called a PFO. Researchers will compare genetic differences and blood flow patterns between 240 adults who have migraine with aura, some with a PFO and some without. No new trea…
Sponsor: Azienda Usl di Bologna • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:04 UTC
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500 patients join hunt for genetic clues in brain vessel disease
Knowledge-focused Recruiting nowThis study is following 500 people with cerebral small vessel disease (CSVD) to see how their genes affect their brain scans, symptoms, and health over time. Participants get genetic testing and MRI scans at the start and again after 1-2 years. The goal is to better understand th…
Sponsor: National Taiwan University Hospital • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:13 UTC
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Scientists launch major effort to unlock secrets of rare brain disease CADASIL
Knowledge-focused Recruiting nowThis study follows 660 adults with CADASIL, a genetic condition that causes strokes and dementia, for up to 5 years. Researchers will use brain scans, memory tests, and blood samples to track how the disease progresses from its earliest stages. The goal is to identify factors tha…
Sponsor: University of Wisconsin, Madison • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:11 UTC
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Massive leukodystrophy biobank aims to unlock disease secrets
Knowledge-focused Recruiting nowThis study collects medical information and biological samples (like blood or tissue) from up to 12,000 people with leukodystrophies—rare disorders that damage the brain's white matter. Researchers will use this data to find new genetic causes, develop biomarkers for future trial…
Sponsor: Children's Hospital of Philadelphia • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:55 UTC
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Help unlock the secrets of a rare brain disease by joining this registry
Knowledge-focused Recruiting nowThis study creates a list of people interested in CADASIL research. If you have CADASIL, are at risk, or have a loved one with the condition, you can join. Researchers will then invite you to future studies, making it easier to find volunteers and speed up discoveries about this …
Sponsor: University of Wisconsin, Madison • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:54 UTC