Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
ID06244472

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

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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

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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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