Status:
UNKNOWN
Cognitive Assessment by the Mean of Event Related Potentials
Lead Sponsor:
University Hospital, Limoges
Conditions:
Brain Injuries
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
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 ...
Detailed Description
In order to test the relevance of theoretical models of cognitive functions, examination of patients with cerebral lesions is of great interest. Thus, the goal of this study is to assess cognitive pro...
Eligibility Criteria
Inclusion
- Control subjects
- 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
- 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
Key Trial Info
Start Date :
July 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 1 2018
Estimated Enrollment :
320 Patients enrolled
Trial Details
Trial ID
NCT01899924
Start Date
July 1 2013
End Date
July 1 2018
Last Update
March 10 2015
Active Locations (1)
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1
CHU of Limoges
Limoges, France, 87042