Informations générales (source: ClinicalTrials.gov)
Cognitive Assessment of Patients With Brain Injuries by the Mean of Event (PEC)
Interventional
N/A
University Hospital, Limoges (Voir sur ClinicalTrials)
juillet 2013
juillet 2018
29 juin 2024
The main objective of this study is to describe differential cognitive processing of
various stimuli by a population of control subjects and a population of patients with
selective cognitive deficits or altered states of consciousness by using dedicated ERP
paradigms and high-density EEG picked up system.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| CHU of Limoges - 87042 - Limoges - France | Frederic Faugeras, Dr | Contact (sur clinicalTrials) | |||
Critères
Tous
Control subjects
Inclusion Criteria:
- adults between 18 and 80,
- written informed consent obtained from the subject,
- covers by social insurance,
- absence of psychoactive drug intake in the week preceding the examination or alcohol
intake the day before the exam
Exclusion Criteria:
- pregnant patients or breastfeeding,
- sensory deficit incompatible with the participation in tne study,
- person under a legal protection measure, under guardianship,
- psychoactive drug intake in the week preceding the examination or alcohol intake the
day before the exam
Patients :
Inclusion Criteria:
- adults between 18 and 80,
- written informed consent obtained from the patient or his relatives,
- covers by social insurance,
- patients with either focal or diffuse brain damage drom trauma, vascular, tumor or
other aetiologies, or with a history of neonatal or congenital diseases,
- patients with selective cognitive disorders or with altered states of consciousness
Exclusion Criteria:
- Pregnant patients or breastfeeding,
- sensory deficit incompatible with the participation in the study
Inclusion Criteria:
- adults between 18 and 80,
- written informed consent obtained from the subject,
- covers by social insurance,
- absence of psychoactive drug intake in the week preceding the examination or alcohol
intake the day before the exam
Exclusion Criteria:
- pregnant patients or breastfeeding,
- sensory deficit incompatible with the participation in tne study,
- person under a legal protection measure, under guardianship,
- psychoactive drug intake in the week preceding the examination or alcohol intake the
day before the exam
Patients :
Inclusion Criteria:
- adults between 18 and 80,
- written informed consent obtained from the patient or his relatives,
- covers by social insurance,
- patients with either focal or diffuse brain damage drom trauma, vascular, tumor or
other aetiologies, or with a history of neonatal or congenital diseases,
- patients with selective cognitive disorders or with altered states of consciousness
Exclusion Criteria:
- Pregnant patients or breastfeeding,
- sensory deficit incompatible with the participation in the study