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NCT06466681Recruiting

Changes in Attentional Control After a Focal Seizure.

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
21 May 2024
Start date
4 Mar 2024
Primary completion date
9 Mar 2027
Lead sponsor
University Hospital, Lille
Diseases
Epilepsy
NCT number
NCT06466681

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 4 Mar 2024 to the primary completion date, 9 Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Absence of any epileptic seizure recorded during the hospitalization
  • Recurrent seizures preventing the recording of at least 24 hours without any seizure following a seizure.

Other

  • Pregnancy or breastfeeding
  • Not able to give consent (Article 1121-8 of the CSP)
  • Vulnerable person
  • Being deprived of liberty by judicial or administrative decision (Article L 1121-6 of the CSP)
  • Guardianship
  • Have a high probability of not respecting the protocol or of abandoning the study

Who the study is looking for

  • Age superior to 18 and under 80
  • Focal epilepsy with indication to pre-surgery work-up and 5 days programmed hospitalization dedicated to this work-up
  • Normal global cognitive performance (standard progressive Raven matrices score \> 5th percentile)
  • Be affiliated to the social security system
  • Have signed an informed consent

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital,
Coordinator of this site? Confirm its status
LilleFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.