NCT04694313

Brief Summary

This research is a feasibility study on a new generation of brain magnetic activity sensor which should allow the development of this modality, until now limited by its cost to a few large university centers. The measurement of magnetic activity allows the detection and localization of abnormal activities such as paroxysmal events occurring between seizures in patients with epilepsy as well as research into brain function. It is the only one, along with EEG and related techniques, to provide data related to the speed of the brain. MEG, by virtue of the properties of magnetic fields, has a greater potential than EEG for the detection and localization of the neuronal sources which cause it. The MEG sensors used until now use Superconducting Quantum Interference Devices (SQUID) components that are extremely sensitive but require complex instrumentation and only operate under superconducting conditions, resulting in prohibitive maintenance and cost. The alternative could come from a new magnetic activity sensor: the optical pumping magnetometers of the alkaline type. This preliminary study proposes to compare SQUID sensors with MPO He4 sensors for their ability to detect abnormal activities recorded in epileptic patients. Measurements that cannot be recorded simultaneously Two types of measurement will be compared with the reference that constitutes in-depth recording (Stereotactic-EEG or SEEG) used to precisely define the region of the brain to be resected in order to cure epileptic patients of their seizures. The expected results are a capacity of this type of sensors to detect epileptic activities equivalent to that of SQUIDs.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2021

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 30, 2020

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 5, 2021

Completed
1 month until next milestone

Study Start

First participant enrolled

February 18, 2021

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2022

Completed
Last Updated

April 15, 2026

Status Verified

April 1, 2026

Enrollment Period

1.8 years

First QC Date

December 30, 2020

Last Update Submit

April 11, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Signal to noise ratio visible on the sensors

    Interictal peaks or oscillations in different frequency bands (gamma, ripples, fast ripples)

    Visit 0 at month 0

Study Arms (1)

OPM

EXPERIMENTAL

Two types of measurement will be compared (SQUID and OPM) with the reference that constitutes the in-depth recordings (Stereotactic-EEG or SEEG) used to precisely define the region of the brain to be resected in order to cure epileptic patients of their seizures.

Device: OPM

Interventions

OPMDEVICE

Simultaneous MEG SQUID + SEEG acquisition followed by a simultaneous MEG OPM + SEEG acquisition.

OPM

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adult patient (≥ 18 years old)
  • Patient with drug-resistant focal epilepsy, undergoing SEEG exploration
  • Healthy subject, devoid of central neurological pathology, major ((≥ 18 years)
  • Patient or healthy subject capable of giving informed consent for the study

You may not qualify if:

  • MEG "incompatible" healthy patients or volunteers.
  • Wearers of prosthesis or pacemaker likely to generate artefacts interfering with the measurement. There is no danger to the subject, but the measurement itself may be impossible.
  • Patients or healthy volunteers who cannot stand standing still for a few minutes.
  • Pregnant or breastfeeding women
  • Adults under guardianship or under legal protection
  • People deprived of their liberty
  • People who have not signed the informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Epileptology and Cerebral Rhythmology, Hôpital La Timone, APHM

Marseille, 13885, France

Location

Related Publications (1)

  • Badier JM, Schwartz D, Benar CG, Kanzari K, Daligault S, Romain R, Mitryukovskiy S, Fourcault W, Josselin V, Le Prado M, Jung J, Palacios-Laloy A, Romain C, Bartolomei F, Labyt E, Bonini F. Helium Optically Pumped Magnetometers Can Detect Epileptic Abnormalities as Well as SQUIDs as Shown by Intracerebral Recordings. eNeuro. 2023 Dec 22;10(12):ENEURO.0222-23.2023. doi: 10.1523/ENEURO.0222-23.2023. Print 2023 Dec.

MeSH Terms

Conditions

Epilepsy

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System Diseases

Study Officials

  • François CREMIEUX

    Assistance Publique Hôpitaux de Marseille

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 30, 2020

First Posted

January 5, 2021

Study Start

February 18, 2021

Primary Completion

December 1, 2022

Study Completion

December 1, 2022

Last Updated

April 15, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share

Locations