Actively Recruiting
Local Field Potentials in Dystonia
Led by Newcastle-upon-Tyne Hospitals NHS Trust · Updated on 2025-12-30
25
Participants Needed
1
Research Sites
169 weeks
Total Duration
On this page
Sponsors
N
Newcastle-upon-Tyne Hospitals NHS Trust
Lead Sponsor
M
Medtronic
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn whether local field potential (LFP) signals recorded from the globus pallidus interna (GPi) using the Medtronic Percept™ deep brain stimulation (DBS) device can help optimize DBS programming for people with dystonia. The study will also explore whether LFP patterns can serve as a biomarker of disease activity and predict treatment response. The main questions it aims to answer are: Do LFP peaks in the alpha-theta range reliably correlate with dystonia severity and clinical characteristics? Can LFP-based programming achieve similar or better clinical outcomes compared to traditional programming methods? How do LFP profiles change with stimulation and other treatments such as botulinum toxin or oral medications? Researchers will compare two programming approaches: Traditional programming based on clinical assessment and imaging. LFP-guided programming based on the site and characteristics of LFP peaks Participants will: Undergo DBS surgery for dystonia as part of standard clinical care. Attend regular follow-up visits for DBS programming and outcome assessments. Complete clinical rating scales for dystonia severity, quality of life, cognition, and mood. Take part in neurophysiological assessments, including surface EMG, EEG, and reaction time tasks. Have LFP recordings collected using the Medtronic Percept™ device during clinic visits and, where possible, at home using device sensing features. This study will help determine whether LFP analysis can shorten the time to optimal DBS settings and improve outcomes for people with dystonia.
CONDITIONS
Official Title
Local Field Potentials in Dystonia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older at screening.
- Clear clinical diagnosis of primary dystonia (idiopathic or genetic forms).
- Candidate for GPi DBS surgery for dystonia treatment.
- Able to provide informed consent.
You will not qualify if you...
- Significant neurological or psychiatric disorder (including dementia) that would interfere with outcome evaluation.
- Participation in a therapeutic research trial within the last year.
- Diagnosis of functional (psychogenic) dystonia.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinical Ageing Research Unit,
Newcastle upon Tyne, Tyne & Wear, United Kingdom, NE4 6BE
Actively Recruiting
Research Team
D
David Ledingham, MA, MBBS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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