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Study identifier: NCT07325487 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Interposed Nucleus aDBS for Ataxia

Condition: Spinocerebellar Ataxia (SCA) · Spinocerebellar Ataxia Type 6  ·  Sponsor: University of Florida

PhaseNA
Planned participants5
Who can joinAll sexes, 21 Years to 89 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Julia C Gonzalez, BA  ·  (352) 265-0111  ·  Julia.Gonzalez@neurology.ufl.edu

Emily Rafferty, PhD  ·  Emily.Rafferty@neurology.ufl.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Norman Fixel Institute for Neurological DiseasesGainesville, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07325487