Deep Brain Stimulation for Spinocerebellar Ataxia
NCT07288437 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5
Last updated 2026-03-18
Summary
The goal of this clinical trial is to test the safety of placing Deep Brain Stimulators (DBS) in the cerebellum and using electrical stimulation of that part of the brain to treat symptoms related to the participants spinocerebellar ataxia. Five adults diagnosed with spinocerebellar ataxia type 6 (SCA6) with inadequate cerebellar symptom relief will be implanted with a Medtronic Percept Primary Cell Neurostimulator. The device will be implanted into the dentate nucleus, which is a structure located within the cerebellum that is responsible for controlling movement and balance.
Specifically, the investigators will be using adaptive deep brain stimulation (aDBS), which analyzes brain signals and automatically adjusts the strength, timing, and pattern of stimulation according to the patient's needs at any given moment. This study will evaluate the feasibility, safety, and tolerability of aDBS in SCA6 patients.
Conditions
- Spinocerebellar Ataxia (SCA)
- Spinocerebellar Ataxia Type 6
Interventions
- DEVICE
-
Deep Brain Stimulation (DBS)
This device will be surgically implanted into the dentate nucleus of the cerebellum.
Sponsors & Collaborators
-
Raynor Cerebellum Project
collaborator UNKNOWN -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Marta San Luciano Palenzuela, MD, PhD · University of California, San Francisco
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Max Age
- 89 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-03-31
- Primary Completion
- 2029-03-31
- Completion
- 2031-03-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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