Adjustment Exploratory Protocols and Functional Evaluation of New Non Invasive Devices in Patient Volunteers
Not Applicable
Completed
- Conditions
- Neurological Diseases
- Interventions
- Device: Imaging devices
- Registration Number
- NCT02790424
- Lead Sponsor
- University Hospital, Grenoble
- Brief Summary
Parameters, sequences or paradigms optimisation in view of data quality and relevancy improvement.
- Detailed Description
Various tests are needed for methodological optimization of the several devices (per-operative MRI, MEG, EEG, SPECT-CT, motor platform) of the technological platform.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
- Volunteers patient
- Male or female aged over 18 years
- Registered in the French social security scheme
- Signed informed consent
Exclusion Criteria
- Contraindication to Magnetoencephalography (MEG) and/or Electroencephalography (EEG)
- Contraindication to Magnetic resonance imaging (MRI)
- All categories of protected persons
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Patients Imaging devices Imaging devices
- Primary Outcome Measures
Name Time Method Magnetic brain activity 2 hours MEG records
Brain imaging 2 hours MRI and SPECT-CT records
Motor activity parameters 2 hours Motor platform records
Electrical brain activity 2 hours EEG records
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
CLINATEC
🇫🇷Grenoble, France