Multimodal Neuroimaging Analysis After Mild Traumatic Brain Injury
NCT ID: NCT03342612
Last Updated: 2019-02-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
41 participants
INTERVENTIONAL
2016-07-18
2018-01-29
Brief Summary
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In this research, the investigators will develop a unique multi-modal neuroimaging protocols to assess brain changes after minor head trauma and over the time. Investigators want to perform magnetic resonance imaging (MRI) to assess cerebral blood flow using Arteria Spin Labelling (ASL), structural changes using Diffusion Tensor Imaging (DTI), susceptibility weighted imaging (SWI), and functional changes using BOLD resting-functional MRI.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Brain Magnetic Resonance Imaging (MRI)
Neuroimaging protocol to assess brain changes after minor head trauma and over the time.
Brain Magnetic Resonance Imaging (MRI)
Interventions
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Brain Magnetic Resonance Imaging (MRI)
Eligibility Criteria
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Inclusion Criteria
\- Male 18 to 25 years, enrolled in French Social Security.
Group of mTBI patients:
\- Diagnosis of mTBI in the last 2 weeks confirmed in emergency department of Bordeaux CHU, using the WHO definition (2004): "head trauma ≤ 24h with Glasgow Coma Scale score of 13-15 and with one or more of the three symptoms following: confusion or disorientation, loss of consciousness for 30 minutes or less, posttraumatic amnesia for less than 24h".
Group of footballers:
\- Member of the "CFA" and "U19" teams of "Girondins de Bordeaux".
Group of controls:
\- Practicing regular physical activity (excluding combat or contact sports).
Exclusion Criteria
* Drug addiction including alcohol Taking drugs targeting the central nervous system History of head trauma, or other notion of central nervous system injury
* History of severe high blood pressure, diabetes, chronic cardiovascular pathology, progressive or debilitating disease
* Subject unable to give informed consent
* Contraindication to MRI: head circumference\> 60 - Claustrophobia - Pacemaker, Implantable Neurostimulation, Implantable Defibrillator - Cochlear Implants - Ocular or cerebral ferromagnetic foreign body
* Refusal to be informed of an abnormality detected during MRI.
18 Years
30 Years
MALE
Yes
Sponsors
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University Hospital, Bordeaux
OTHER
Responsible Party
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Locations
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University Hospital Bordeaux
Bordeaux, , France
Countries
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Other Identifiers
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CHUBX2016/07
Identifier Type: -
Identifier Source: org_study_id
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