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IRM Cognition in Patients With Head Trauma

U

University Hospital, Clermont-Ferrand

Status

Unknown

Conditions

Brain-damaged Patients

Treatments

Other: Cognitive rehabilitation program

Study type

Observational

Funder types

Other

Identifiers

NCT03181373
CHU-328

Details and patient eligibility

About

Longitudinal descriptive study of a cohort of twenty brain-damaged patients for a two years period.

Full description

The following data are collected in 3 months, 12 months then 24 months after the accident with followed data collection :

  • Clinical, neuropsychological assessments
  • Diffusion magnetic resonance imaging (MRI) for the reconstruction of anatomical pathways
  • Functional imaging data.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients, over the age of 18.
  • Mild traumatic brain injury (Initial Glasgow score between 9 and 12)
  • Severe brain injury (Initial Glasgow score between 3 and 8),
  • Diffuse axonal injury and/or focal lesions.

Exclusion criteria

  • Patients with MRI contraindications,
  • Antecedents of brain lesions,
  • Important lesions of the lobes and cortex on cerebral CT,
  • Anoxic lesions related to cardiorespiratory arrest,
  • Must be able to perform neuropsychological tests,
  • Visual and auditory impairments.
  • Aphasia

Trial design

20 participants in 1 patient group

Traumatic brain injury population
Description:
Defined population : traumatic brain injury population
Treatment:
Other: Cognitive rehabilitation program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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