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Frontosubthalamic Networks in Parkinson's Disease.

Sponsor: University of Oxford

NCT ID: NCT06485986

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
DBS on/off (other)
How long the study runs
Study runs about 26 months (dates as stated)
About the drug or intervention
DBS on/off — other: DBS will be turned on and off for experimental periods to compare the effect of DBS on behaviour.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
20
Started
2024-06-01
Last checked
2025-03

Plain English Summary

What is this study?

  • • Testing a new treatment for parkinson disease
  • • NA - 20 participants
  • • The goal of this experimental study with is to understand the underlying mechanisms behind the increase in impulsivity seen in some patients that undergo deep brain stimulation of the subthalamic nucleus for Parkinson's Disease

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with parkinson disease

Where?

  • • Oxford - John Radcliffe Hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The goal of this experimental study with is to understand the underlying mechanisms behind the increase in impulsivity seen in some patients that undergo deep brain stimulation of the subthalamic nucleus for Parkinson's Disease. The main questions it aims to answer are: What are the distributed network effects of deep brain stimulation to the subthalamic nucleus? How does this correlate with increased impulsivity? Can alternative stimulation settings be used to minimize these? Participants will complete decision-making tasks whilst their deep brain stimulation devices are turned on and off with simultaneous magnetoencephalography recordings (a type of non-invasive brain scan that measures brain activity in real-time)

Parkinson DiseaseImpulse Control Disorder

How this trial compares with your answers

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Treatment history

Treatments you must have had:

  • ✓ implanted STN electrodes for DBS in addition to their dopamine replacement therapy

What the study is looking for

  • ✓Participant is willing and able to give agreement to take part for participation in the study.
  • ✓Male or Female, aged 18 years or above.
  • ✓Diagnosed with Parkinson's disease who have required implanted STN electrodes for DBS in addition to their dopamine...
  • ✓Diagnosed with or without (control group) impulse control disorders since the diagnosis of Parkinson's Disease.
  • ✓Participant willing and able to sit in the MEG scanner and follow instructions.

Who cannot take part

  • ✗Patients with extreme language barrier that cannot understand the purpose or instructions of the study despite the...
  • ✗Other implanted medical devices that may cause artefacts during MEG recordings.
  • ✗Participants with a history of co-morbid neurological disorders.
  • ✗Participant enrolled onto another clinical trial related to a neurological disorder (including Parkinson's disease)...
  • ✗Participants who are unable to sit still in a MEG scanner for the duration of this experiment e.g. patients with...
See the full criteria
Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the study. * Male or Female, aged 18 years or above. * Diagnosed with Parkinson's disease who have required implanted STN electrodes for DBS in addition to their dopamine replacement therapy. * Diagnosed with or without (control group) impulse control disorders since the diagnosis of Parkinson's Disease. * Participant willing and able to sit in the MEG scanner and follow instructions. * Participant willing and able to delay their morning dose of dopamine replacement therapy for up to four hours (180 minutes experimental time + journey time). Exclusion Criteria: * Patients with extreme language barrier that cannot understand the purpose or instructions of the study despite the use of an interpreter. * Other implanted medical devices that may cause artefacts during MEG recordings. * Participants with a history of co-morbid neurological disorders. * Participant enrolled onto another clinical trial related to a neurological disorder (including Parkinson's disease) that may interfere with the results of this study. * Participants who are unable to sit still in a MEG scanner for the duration of this experiment e.g. patients with chronic pain or osteoarthritis. This will be assessed with their primary clinician

Where Is This Study? (1 UK site)

John Radcliffe Hospital

Oxford OX39DU, United Kingdom

Recruiting
Site contact (verified)
John Eraifej, BSc MBChB MRCS01865222763

How to Get in Touch

John Eraifej, BSc MBChB MRCS

Sponsor contact

CONTACT

01865222763 john.eraifej@ndcn.ox.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-03