Actively Recruiting

Age: 18Years - 80Years
All Genders
NCT06466681

Changes in Attentional Control After a Focal Seizure.

Led by University Hospital, Lille · Updated on 2026-04-27

100

Participants Needed

1

Research Sites

157 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Epilepsy is frequently associated with cognitive and attentional disorders. Several studies have pointed out that there are modifications of brain activity in resting state during peri-ictal period in EEG and functional MRI. However, to date, no study has assessed the changes in attentional control after a seizure. The investigators hypothesize that a localized discharge is associated with a disorganization of the networks engaged in attentional control. In this regard, the investigators propose a prospective longitudinal study assessing the changes in attentional control after a focal seizure.

CONDITIONS

Official Title

Changes in Attentional Control After a Focal Seizure.

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age superior to 18 and under 80
  • Diagnosed with focal epilepsy with indication for pre-surgery evaluation
  • Scheduled for a 5-day hospitalization dedicated to pre-surgery work-up
  • Normal global cognitive performance (standard progressive Raven matrices score > 5th percentile)
  • Affiliated to the social security system
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding
  • Unable to give consent
  • Vulnerable person
  • Deprived of liberty by judicial or administrative decision
  • Under guardianship
  • High probability of not following the study protocol or dropping out
  • No epileptic seizure recorded during hospitalization
  • Frequent seizures preventing 24-hour seizure-free recording after a seizure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital,

Lille, France, 59000

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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