Clinical Trial

Interposed Nucleus aDBS for Ataxia

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Summary
This is a single-center, open-label study designed to evaluate the feasibility, safety, and preliminary efficacy of cerebellar adaptive deep brain stimulation (aDBS) in adults with spinocerebellar ataxia type 6 (SCA6). A total of 5 participants will be enrolled. Participants will undergo surgical implantation of deep brain stimulation (DBS) leads targeting the motor interposed nucleus of the cerebellum. The leads will be connected to one or two implantable pulse generators capable of delivering stimulation to deep brain structures and recording neural activity. Participants will complete up to 18 in-person study visits over a 24-month follow-up period. During these visits, neural signals will be recorded under varying behavioral tasks and stimulation conditions. Early study visits will be used to identify optimal stimulation parameters and neural biomarkers associated with disease state. These biomarkers will subsequently be used to implement adaptive DBS, in which stimulation amplitude is automatically adjusted in response to recorded neural activity. Study outcomes will include assessments of safety and feasibility of cerebellar aDBS, as well as preliminary evaluation of its effects on clinical measures.
Protocol Amendment History 3 changes
critical Recruitment opened 2026-06-30
notable Primary completion pushed: 2031-03 -> 2031-06 2026-06-30
minor Completion pushed: 2031-03 -> 2031-06 2026-06-30
Trial Details
NCT Number NCT07325487
Lead Sponsor University of Florida
Collaborators: Raynor Cerebellum Project
Conditions Spinocerebellar Ataxia (SCA), Spinocerebellar Ataxia Type 6
Enrollment 5 participants
Start Date 2026-06-02
Primary Completion 2031-06 (estimated)
Study Completion 2031-06 (estimated)
Updated on ClinicalTrials.gov 2026-07-20