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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History Study of and Genetic Modifiers in Spinocerebellar AtaxiasCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyskinesias, Machado-Joseph disease, Neurologic Manifestations, Spinocerebellar Ataxias, Spinocerebellar Degenerations, Spinocerebellar ataxia 8, atactic disorder, non-human animal, brain disorder, central nervous system disorder, cerebellar ataxia, cerebellar disorder, hereditary disease, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, spinal cord disorder, spinocerebellar ataxia 7, spinocerebellar ataxia type 1, spinocerebellar ataxia type 10, spinocerebellar ataxia type 2, spinocerebellar ataxia type 6, spinocerebellar ataxia type 8RecruitingNot stated2026-08-03NCT01060371

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Research sitesCityCountryLinked trials
Columbia UniversityNew YorkUnited States154
Emory UniversityAtlantaUnited States1
Harvard UniversityBostonUnited States1
Houston MethodistHoustonUnited States63
John Hopkins UniversityBaltimoreUnited States14
Le Centre hospitalier de l'Université de MontréalMontrealCanada1
Nortwestern UniversityChicagoUnited States1
University of California Los AngelesLos AngelesUnited States87
University of California San FranciscoSan FranciscoUnited States27
University of ChicagoChicagoUnited States312
University of FloridaGainesvilleUnited States144
University of MichiganAnn ArborUnited States538
University of MinnesotaMinneapolisUnited States325
University of PennsylvaniaPhiladelphiaUnited States23
University of South FloridaTampaUnited States33
University of Texas Southwestern Medical CenterDallasUnited States249
University of WashingtonSeattleUnited States172