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
NA
10 participants
INTERVENTIONAL
2023-05-03
2026-05-03
Brief Summary
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The arrival on the market of the PERCEPT™ (new stimulator/recorder, Medtronic, Minneapolis, USA) now allows, in addition to the stimulation delivery, the recording of intracerebral activity at a distance from surgery, in a non-invasive way and in ecological condition at home. Investigators aim at recording the variations of thalamic Local Field Potentials (LFP) oscillations, in ecological condition, during rest and movement, with and without deep brain stimulation, once a week, between M3 and M6 post surgery.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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experimental arm
Patient with ET and Receiving deep brain stimulation treatment with implantation of the PERCEPT™ device
Recordings of thalamic activity
Recordings of thalamic activity will be performed at home, in ecological conditions. They will be realized during 4 distinct conditions each week between M3 and M6 post implantation: at rest and during tremor-induced movements. For these recordings, stimulation will be either turned Off or On. Three successive recordings of 30 seconds separated by 1 minute will be made for each condition.
Interventions
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Recordings of thalamic activity
Recordings of thalamic activity will be performed at home, in ecological conditions. They will be realized during 4 distinct conditions each week between M3 and M6 post implantation: at rest and during tremor-induced movements. For these recordings, stimulation will be either turned Off or On. Three successive recordings of 30 seconds separated by 1 minute will be made for each condition.
Eligibility Criteria
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Inclusion Criteria
* Receiving deep brain stimulation treatment with implantation of the PERCEPT™ device according to standard care
* Chronic progressive cardiac, renal, hematological or pulmonary diseases under treatment.
* Patient aged between 18 to 75 years
* Normal brain MRI
* MATTIS score ≥ 130/144 or MOCA ≥ 24/30
* Subject affiliated with or benefiting from a social security plan
* Free, informed and written consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research)
Exclusion Criteria
* MRI showing significant brain atrophy or significant hypersignals
* Pregnant or breastfeeding women
* Being unable to give personal consent
* Be subject to a measure of legal protection (curatorship, guardianship) or placed under judicial protection.
18 Years
75 Years
ALL
No
Sponsors
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MINDig
UNKNOWN
University Hospital, Bordeaux
OTHER
Responsible Party
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Principal Investigators
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Dominique GUELH, Pr
Role: STUDY_DIRECTOR
University Hospital, Bordeaux
Edouard COURTIN, Dr
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Bordeaux
Mahmoud HASSAN, Dr
Role: STUDY_CHAIR
MINDig
Locations
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CHU de Bordeaux
Bordeaux, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CHUBX 2022/29
Identifier Type: -
Identifier Source: org_study_id
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