Study of the Intracerebral Electrophysiological Signature in the Epileptic Patient

ConditionEpilepsy
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorUniversity Hospital, Toulouse

About this trial

As part of the clinical management of certain severe, drug-resistant forms of epilepsy, it is necessary to implant electrodes in the brain to identify the epileptic network prior to potential neurosurgical resection of the source zones. This standardized procedure, known as Stereo-Electroencephalography (SEEG), was developed in France in the 1960s. The electrodes remain implanted for several days-typically two weeks-while awaiting spontaneous epileptic seizures. During this period, the patient remains hospitalized, and their electroencephalographic activity is recorded around the clock.

Patients can be asked to perform cognitive tasks (such as tasks involving memory, attention, vision, language, and decision-making) while awake or asleep; the results can then be correlated with the intracerebral electroencephalographic activity recorded simultaneously as part of their clinical care. This approach makes it possible to capture the electrophysiological signatures of specific cognitive processes, thereby enabling researchers to: 1) create a brain map of electrophysiological signatures, 2) improve standard models of cognitive function, and 3) study the dysfunction of these processes in epilepsy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient with drug-resistant focal epilepsy undergoing SEEG evaluation as part of the pre-surgical workup for epilepsy

Intellectual capacity sufficient to perform cognitive tasks, receive information about the study procedure, and understand the information sheet

Disqualifiers

Patients already participating in another research project that prohibits participation in another study

Trial population

patients with drug-resistant epilepsy hospitalized for stereo-electroencephalography

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Cognitive tasks in the form of questionnaires

    Other intervention

    During their hospitalization for SEEG, patients will perform cognitive tasks to assess memory, vision, attention, language, and decision-making.

Treatment groups

75 Participants
are divided into 1 treatment group
Group A: Patients hospitalized for SEEG with cognitive tasks1 intervention

Trial outcomes

Primary outcomes

1

Construction of a database of electrophysiological signatures of various cognitive functions

Correlation of performance on a task involving a neurocognitive process with characteristics of brain activity recorded during the task (electrophysiological signature) using intracranial stereo-electroencephalography (SEEG) electrodes.

Time frame
3 weeks after the inclusion

Secondary outcomes

1

Evaluation of the impact of epilepsy on these electrophysiological signatures

Significant impact of the patient's epilepsy on the normal electrophysiological signature expected during certain cognitive processes.

Time frame
3 weeks after the inclusion
2

Determine whether a given brain region is dysfunctional in certain epileptic patients by comparing it with the atlas of normal physiological signatures.

Identification of a dysfunctional brain region in an epileptic patient if the electrophysiological signature differs significantly from that expected based on the atlas.

Time frame
3 weeks after the inclusion

Other outcomes

Sponsors and contacts

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