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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Biological Collection of the Rare Diseases of the Brain and Eye Vessels Cohort - 2Cardiovascular Abnormalities, Cavernous Sinus Syndromes, Central Nervous System Vascular Malformations, Cerebral Small Vessel Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Infarction, Necrosis, Neoplasms by Histologic Type, Pathologic Processes, Pathological Conditions, Signs and Symptoms, brain disorder, brain infarction, brain ischemia, cardiovascular disorder, cavernous hemangioma, central nervous system disorder, central nervous system malformation, cerebral arterial disease, cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1, cerebral infarction, cerebrovascular disorder, dementia, hemangioma, hematologic disorder, hemorrhagic disease, hereditary disease, intracranial arterial disease, ischemic disease, neoplasm, nervous system disorder, stroke disorder, vascular cancer, vascular dementia, vascular disorder, vascular hemostatic disease, vascular malformationNot yet recruitingNot applicable2026-06-16NCT07650110

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Assistance Publique - Hôpitaux de Paris985

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