Deep Brain Stimulation for Visuomotor Function in Parkinson's Disease
NCT ID: NCT05400499
Last Updated: 2026-01-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
40 participants
OBSERVATIONAL
2022-10-04
2026-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Parkinson's disease with DBS
This is the only group. The patients in this group will have bilateral subthalamic region deep brain stimulator. They will be recruited after they are therapeutically optimized on stimulation as well as medical therapy.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Availability of pre-operative MR images (with a T1-weighted, gradient-echo sequence) and ability to get post-operative MRI or CT scans
* Hoehn and Yahr stage 2-4 when off medication, and a stable antiparkinsonian medication regimen and DBS parameter settings
Exclusion Criteria
* Dementia
* Clinically significant untreated depression or anxiety
* Clinical features suggestive of atypical parkinsonism
ALL
No
Sponsors
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VA Office of Research and Development
FED
Responsible Party
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Principal Investigators
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Aasef G. Shaikh, MD PhD
Role: PRINCIPAL_INVESTIGATOR
Louis Stokes VA Medical Center, Cleveland, OH
Locations
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Louis Stokes VA Medical Center, Cleveland, OH
Cleveland, Ohio, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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N3878-P
Identifier Type: -
Identifier Source: org_study_id
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