CADASIL Registry Study
Recruiting now
Conditions studied: Cadasil
In brief
The aim of this study is to determine the clinical spectrum and natural progression of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) and related disorders in a prospective multicenter study, to assess the clinical, genetic and epigenetic features of patients with CADASIL , to optimize clinical management.
Key facts
- Study ID
- NCT04310098
- Run by
- Bin Cai
- People needed
- 1000
- Starts
- 2020-03-09
- Expected to finish
- 2049-03-09
- Last updated by the study team
- 2023-09-28
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Sign informed consent.
- Age>18
- Clinical diagnosis of patients with CADASIL,and confirmed by genetic test or skin biopsy
- Asymptomatic NOTCH3 mutation carriers
- Relatives of CADASIL patients or carriers
- Unrelated healthy controls
You may not qualify if…
- Unable to cooperate with inspectors
- Serious systemic illness, such as heart, liver, kidney disease or major mental illness
- Contraindications for imaging examination
Where it is running
- Department of Neurology , First Affiliated Hospital Fujian Medical University — Fuzhou, Fujian, China (enrolling)
Full record on ClinicalTrials.gov
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