Actively Recruiting
Towards a New Generation of Magnetoencephalographs: Evaluation of the FYNA Research (Mag4Health 48 Sensors MEG's Name) System Full-head Magnetoencephalographs System With Optically Pumped Magnetometers
Led by Hospices Civils de Lyon · Updated on 2026-06-01
80
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new generation of magnetoencephalography (MEG) devices that use optically pumped magnetometers with Helium 4 to record brain magnetic activities. The study includes healthy adults and male athletes who have suffered a mild concussion. The goal is to compare this new device's ability to detect and map brain activity with that of classical MEG systems, focusing on brain responses to visual, auditory, somatosensory, and motor stimuli. Participants will undergo several experiments using the FYNA Research MEG system. Healthy volunteers will complete tasks involving visual and auditory attention, language production, rest, and visuo-motor activities. Concussed athletes will have their resting brain activity recorded to assess frequency modulations. The study compares signal-to-noise ratios and brain activity maps from the new device with those from classical MEG during these tasks. During the study, participants will visit once for inclusion and then return within 1 to 30 days for MEG recordings and assessments. Researchers will measure signal quality, brain activity mapping, and participant comfort through questionnaires after recording sessions. The study monitors safety and participant experience, aiming to gather detailed data on the new MEG device's performance. Total participation time depends on scheduling within the defined visit window.
CONDITIONS
Brief Title
A New Generation of Magnetoencephalographs for High Speed Functional Brain Imaging
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy volunteers aged 18 to 70 years
- Male athletes aged 18 to 40 years with mild concussion confirmed by a club doctor and neurologist within three weeks
- Strong motivation to participate in the study
- Signed informed consent for the study
You will not qualify if you...
- Major cognitive deficits preventing understanding of instructions
- Previous neurological, psychiatric, or sleep disorders (except mild concussion for athletes)
- Positive pregnancy test during inclusion
- Under guardianship, curatorship, or legal protection
- Deprived of liberty
- Not affiliated with a social security system
- Refusal to be informed of abnormalities detected during MEG and MRI
- Contraindications to MEG and MRI, including metal implants (pacemaker, neurostimulator, cochlear implant, metallic prosthesis, intracerebral clip, dental appliances, ferromagnetic foreign bodies, ventriculoperitoneal valve) and claustrophobia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 to 30 days
Participants undergo brain imaging sessions using the FYNA Research system during various tasks including visual, auditory, language production, rest, and visuo-motor tasks to evaluate the system's performance.
1 visit (in-person) during which multiple tasks are performed
Trial Site Locations
Total: 2 locations
1
Service de Neurologie Fonctionnelle et d'Epileptologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon
Bron, France, 69677
Actively Recruiting
2
Centre Orthopédique Paul Santy
Lyon, France, 69008
Not Yet Recruiting
Research Team
J
Julien JUNG, MD
D
Denis SCHWARTZ
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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