Monitoring the Alterations That Occur in the Brain Following Traumatic Brain Injury (TBI)

ElMindA

Status: Completed

Conditions: Traumatic Brain Injury (TBI)

Treatments: Device: fMRI

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT02878577

ELM-37

Details and patient eligibility

About

This project, will combine the data collected from existing and innovative technologies: fMRI scans, mapping brain connectivity using EEG in combination with eye-tracking technology (the BNA technology developed by ELMINDA), characterizing of cortical layers using magnetic resonance (the CoLI technology developed by Tel-Aviv University), and DTI imaging (imaging of brain tracks). To do so, Sheba's Medical Center, Tel Hashomer, joined the project and is responsible for recruiting patients from the Department of Neurosurgery and Department of Rehabilitation and also is responsible for performing the needed tests.

Full description

This research project is the continuation of the NOFAR project, collaboration between ELMINDA and Tel-Aviv University, which included a proof of concept of the technology developed in the university to characterize cortical layers using magnetic resonance. In light of the promising results, the partners have decided to make another leap forward, and test the technology amongst specific patient population who suffered a brain trauma (traumatic brain injury, TBI).

Early and proper diagnosis of brain injury is critical, since it can prevent further complications to the patient's health. The tests that are currently available are limited in their ability to provide a comprehensive and accurate assessment of the injured brain: imaging exams such as CT, MRI and PET help identify the location and severity of the injury but cannot provide data on the cognitive and functional effects of the injury. On the other hand, neuropsychological tests only allow examination of current cognitive functioning, and cognitive decline quantification is done according to mathematical models and subjective assessments of the patient and his family. Therefore, this area is lacking and it is important to find an objective measure that enables quantification of brain injury that will be an indication of cognitive decline.

The current project, will last two years, and will combine the data collected from existing and innovative technologies: fMRI scans, mapping brain connectivity using EEG in combination with eye-tracking technology (the BNA technology developed by ELMINDA), characterizing of cortical layers using magnetic resonance (the CoLI technology developed by Tel-Aviv University), and DTI imaging (imaging of brain tracks). To do so, Sheba's Medical Center, Tel Hashomer, joined the project and is responsible for recruiting patients from the Department of Neurosurgery and Department of Rehabilitation and also is responsible for performing the needed tests.

The product that will be developed at the end of the Magneton project is expected to be a unique analysis method that allows examination and monitoring of the affected brain in both a functional and anatomically-structural ultra-high resolution.

Enrollment: 68 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Had the Glasgow coma scale score of 3-15 after the incident. (group 1)
2. males and females Age: 18-60 (not during their military service).

Exclusion criteria

• History of neurological disorders, mental retardation or a previous head injury.
• Current diagnosis or history of psychiatric disorders.
• Drugs and / or alcohol dependence or abuse existed prior to the head injury.
• Unconsciousness.
• Pregnancy.
• Artificial respiration.
• Renal failure.
• Cardiovascular instability.
• Metabolic instability (water, electrolytes, sugar).
• Fever or evidence of microbiological pollutant.
• Uncontrolled seizures.
• Hydrocephalus.
• Patients with open wounds that are not bandaged, preventing the use of the EEG cap.
• Deafness or blindness.
• History of drugs that affect the nervous system in the 3 months prior to the injury.
• Inability to cooperate in carrying out the necessary tests

Trial design

68 participants in 2 patient groups

EEG fMRI TBI Mild/Moderate-Severe severity

Description:

patient population who suffered a brain trauma (traumatic brain injury, TBI). with a Glasgow Coma Scale between 3-15

Treatment:

Device: fMRI

EEG fMRI Control group

Description:

healthy subjects with out a traumatic brain injury

Treatment:

Device: fMRI