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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Neuromodulation to Enhance Motor Function in HSPCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathyRecruitingNot applicable2026-04-22NCT07417943

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Research sitesCityCountryLinked trials
University of KentuckyLexingtonUnited States65