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)

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal is to perform a first evaluation of the capabilities of a new generation of non-invasive magnetoencephalography whole head device using optically pumped magnetometers using Helium 4 as the sensitive element (OPM He4) to record brain magnetic activities. The investigators will record 1) healthy subjects stimulated with visual, auditory, somesthesic and motor stimuli and 2) athletes who suffered a mild concussion. The main hypothesis is that the OPM magnetoencephalographs (MEG) system will be able to detect brain activity. The secondary hypothesis is that the data recorded with the OPM MEG system will allow to reconstruct maps of the brain activity. To test the main hypothesis, they will compare the signal to noise ratio of brain activities between a classical MEG system and the new OPM He4 MEG. The secondary hypothesis will be tested through a comparison of the maps of brain activity obtained thanks to the data recorded with a classical MEG system and the new OPM He4 MEG.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: t
View:

• Age 18 to 70

• Strongly motivated to participate to the study

• Signed informed consent for the study

• Male aged from 18 to 40

• Strongly motivated to participate to the study

• Signed informed consent for the study

• Mild concussion confirmed by the club doctor and a neurologist neurologist in the three weeks preceding the experiment

Locations
Other Locations
France
Service de Neurologie Fonctionnelle et d'Epileptologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon
RECRUITING
Bron
Centre Orthopédique Paul Santy
NOT_YET_RECRUITING
Lyon
Contact Information
Primary
Julien JUNG, MD
julien.jung@chu-lyon.fr
04.72.35.79.00
Backup
Denis SCHWARTZ
denis.schwartz@inserm.fr
04.72.13.89.61
Time Frame
Start Date: 2025-07-09
Estimated Completion Date: 2027-08
Participants
Target number of participants: 80
Treatments
Experimental: Healthy subjects
Healthy volunteers aged between 18 and 70 years, without neurological or psychiatric or sleep disorders
Experimental: Subjects with concussion
Male athletes volunteers with concussion aged between 18 and 40 years, without neurological or psychiatric or sleep disorders other than cerebral concussion.
Related Therapeutic Areas
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov