Sharper MRI could Fine-Tune brain surgery for Parkinson's
NCT ID NCT02800460
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This study tests whether a new, high-field 3T MRI technique can more accurately pinpoint the subthalamic nucleus — a key brain area targeted during deep brain stimulation (DBS) for Parkinson's disease. Researchers will compare images from the new method with standard 1.5T MRI in 105 Parkinson's patients who are candidates for DBS. The goal is to improve surgical precision, which could lead to better symptom relief and fewer side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could improve the precision of deep brain stimulation surgery for Parkinson's, potentially leading to better symptom control and fewer side effects.
- What could go wrong
- This is an early imaging study, not a treatment trial. The new MRI method may not prove more accurate than current techniques, and any benefit to patients remains uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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105 people
The number who actually took part.
- Started
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Oct 2016
- Finished
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Nov 2025
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of idiopathic Parkinson's disease (according to the criteria of the "United Kingdom Parkinson's Disease Society Brain Bank"; * Age between 18 and 70 years * motor complications in the form of fluctuations in motor state or induced dyskinesias dopaminergic therapy, despite optimal medical treatment; * Excellent responsiveness to levodopa (improved motor UPDRS score of higher than 50% during the acute test with levodopa) * People who voluntarily accepted and intelligently participate in the study (signing a written consent) * Patient receiving social health insurance Exclusion Criteria: * Patients carry an apomorphine pump used in single and continuous treatment; * scalable psychiatric pathology; * Dementia (MMS \<24/30); * Existence of against-indications to MRI (cardiac or neural stimulator, ferromagnetic surgical clips, implants and metal objects, intraocular foreign bodies, pregnancy, claustrophobia). * Persons under guardianship, trusteeship or any other administrative or judicial deprivation of rights and freedom
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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GHPS
Paris, Île-de-France Region, 75651, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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