Skip to content

Study of the Intracerebral Electrophysiological Signature in the Epileptic Patient

Study of the Intracerebral Electrophysiological Signature of Cognitive Processes and Functional Mapping in Patients With Drug-resistant Epilepsy

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07796984
Acronym
ACTELIN 2
Enrollment
75
Registered
2026-09-01
Start date
2026-10-01
Completion date
2031-10-31
Last updated
2026-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Keywords

epilepsy, cognitive task, stereoelectroencephalography

Brief summary

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.

Interventions

OTHERCognitive tasks in the form of questionnaires

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

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Construction of a database of electrophysiological signatures of various cognitive functions3 weeks after the inclusionCorrelation 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.

Secondary

MeasureTime frameDescription
Determine whether a given brain region is dysfunctional in certain epileptic patients by comparing it with the atlas of normal physiological signatures.3 weeks after the inclusionIdentification of a dysfunctional brain region in an epileptic patient if the electrophysiological signature differs significantly from that expected based on the atlas.
Evaluation of the impact of epilepsy on these electrophysiological signatures3 weeks after the inclusionSignificant impact of the patient's epilepsy on the normal electrophysiological signature expected during certain cognitive processes.

Countries

France

Contacts

CONTACTJonathan Curot, PHD
curot.j@chu-toulouse.fr05 61 77 94 88

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026