Evaluation of the Risk of Cognitive Deficit After Surgery of Epilepsy by Dynamic Spectral Imaging (ISD) of the Cognitive Functions in Patients Explored in StereoElectroEncephaloGraphy (SEEG)
ISD SEEG
2 other identifiers
interventional
50
1 country
1
Brief Summary
Epilepsy affects between 0.5 and 0.7% of the European population. Despite the availability of numerous drug treatments, one third of patients still have seizures, which are associated with significant cognitive and social complications and excess mortality. In these patients, surgical treatment to remove the epileptogenic zone (EZ), the region of the brain responsible for seizures, is the only approach that can allow control of the disease. However, before investigating this surgery, investigations have to answer two questions: (i) what is the location and extension of the EZ and (ii) what functional risks, both motor and cognitive, would represent the resection of this Cortical region? As it is a functional surgery, it is in fact inconceivable that the surgery will result in an over-handicap. For these reasons, all candidates for surgery benefit from a complete assessment including imaging examinations, a neuropsychological assessment and a long-term video-EEG recording to record seizures. Nevertheless, in some patients, this assessment does not give us a formal answer. In these subjects, it is then necessary to carry out a second step, consisting of an invasive exploration by implantation of intracerebral electrodes during a stereoencephalography (SEEG). Due to its temporal and spatial resolution, the SEEG allows, besides the precise determination of the EZ, to carry out a functional mapping of the cortical regions likely to be included in cortectomy. Conventionally, this mapping is carried out on the basis of the cortical electrical stimulations applied to the implanted electrodes. If this approach is very robust for exploring primary functions such as motor skills or language, it cannot be used to evaluate more complex cognitive tasks such as face recognition or attention Effective cognitive treatment on a daily basis. This has led to the development in recent years, in Lyon and Grenoble, of a complementary approach to cerebral stimulation: dynamic spectral imaging (ISD). Numerous experimental paradigms have demonstrated that the realization of a cognitive task associates with the generation within the cortical regions involved in its treatment of a particular cortical activity. This activity is characterized by oscillations of the cortical rhythm in high frequencies (\> 30 Hz), called gamma activities. The ISD thus consists in mapping this gamma activity during various cognitive tasks, thus making it possible to study more widely the complexity of the cognitive functions. Correlations between gamma activity and cognitive tasks have so far been exclusively performed in the non-epileptic cortex explored at the periphery of the EA during SEEG. Nevertheless, the cortical oscillatory pattern study associated with a specific cognitive task within the EZ could better anticipate complex cognitive deficits that could be generated by the resection of a cortical region. The main objective of this project is to establish the predictive character of the gamma cortical oscillatory pattern associated with a specific cognitive task on the risk of occurrence of a cognitive disorder after surgery of epilepsy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2017
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 9, 2017
CompletedFirst Posted
Study publicly available on registry
March 29, 2017
CompletedStudy Start
First participant enrolled
June 23, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 23, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 23, 2030
January 21, 2026
January 1, 2026
12.6 years
March 9, 2017
January 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
predictive character of the cortical gamma oscillatory pattern associated with a specific cognitive task on the risk of occurrence of a cognitive disorder after epilepsy surgery
Relation between the presence in the epileptogenic zone of a gamma activation in at least 1 of the cognitive tasks performed during the ISD and the occurrence of a postoperative neuropsychological deficit (Wilcoxon test)
12 months post-surgery compare to preoperative assessment (SEEG)
Secondary Outcomes (5)
database on the dynamics of large cerebral networks underlying the main cognitive functions
pre-surgical assessment (SEEG)
spatio-temporal organization of these networks with that predicted by fMRI
preoperative assessment (SEEG, fMRI and cortical stimulations)
effect of intracerebral electrical stimulations
preoperative assessment (SEEG, fMRI and cortical stimulations)
macro-electrophysiological recordings
12 months post-surgery compare to preoperative assessment (SEEG)
micro-electrophysiological recordings
12 months post-surgery compare to preoperative assessment (SEEG)
Study Arms (1)
Dynamic Spectral Imaging (ISD)
EXPERIMENTALEvaluation of cognitive functions by ISD
Interventions
cerebral stimulation: dynamic spectral imaging (ISD)
Eligibility Criteria
You may qualify if:
- patient adult (18-65 y/o) without legal protection measures
- Patient with a drug-resistant focal epilepsy
- Patient with a SEEG exploration as part of pre-surgical assessment of epilepsy
- patient with a consent form signed
- Intellectual capacities compatible with cognitive tasks and the signing of informed consent
- Affiliation to the social security
You may not qualify if:
- Pregnant women: this is already a contraindication to the realization of a SEEG study
- Subjects under 18 years of age or over 65 years of age
- Patient not suffering from EFPR, or not scheduled for SEEG
- Intellectual capacities incompatible with the cognitive tasks and / or the signature of a consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospices Civils de Lyon
Bron, 69500, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sylvain RHEIMS, MD
Hospices Civils de Lyon
Central Study Contacts
Anne-Laure CHARLOIS
CONTACT
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
March 9, 2017
First Posted
March 29, 2017
Study Start
June 23, 2017
Primary Completion (Estimated)
January 23, 2030
Study Completion (Estimated)
January 23, 2030
Last Updated
January 21, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share