EEG Recording
DeviceEEG recording acquired on BrainScope One device.
NCT Number: NCT04279431
The purpose of the study is to validate the clinical outcome in patients with closed head injuries (GCS 14-15, ages 18-85) who are being evaluated for head trauma, integrating the BrainScope One structural injury classifier (SIC) algorithm, with focus on SIC negative classification. In addition, to assess functional impairment (concussion) in these patients, results from Brain Function Index (BFI) or Concussion Index (CI) algorithms will be used for analysis.
This study is active but is not currently recruiting participants.
Notify Me18 year–85 year
All sexes
Observational
Henry Ford Health System, Detroit, Michigan, United States
BrainScope One incorporates brain electrical activity (EEG, a proven electrophysiological core technology) and other multimodal assessment capabilities in a portable, point-of-care, non-invasive device containing algorithms designed to improve early identification, staging, and optimization of treatment for head injured patients (GCS 13-15) who are suspected of a brain injury. Structural Injury Classifier (SIC) provides objective results that indicate the likelihood of a structural brain injury being present, potentially visible on CT Scan. Brain Function Index (BFI) provides an objective measurement to determine the likelihood and severity of brain function impairment such as that seen in concussion/mTBI. The BFI is presented as a percentile compared to a normal corresponding population. Lastly, the Concussion Index (CI) was derived in the most recent BrainScope concussion assessment clinical study, and it is defined as a multivariate, multimodal index to assess the presence and severity of concussion and has been demonstrated to reliably reflect change over time.
The present study population targets those patients who sustained a head injury, have high GCS scores (14-15) and present mild symptoms, for whom the suspicion of structural brain injury is therefore low. Having a rapid, reliable, and sensitive assessment tool to aid in the triage of patients who are suspected of a traumatically induced structural brain injury could aid in appropriate and timely diagnosis and subsequent medical care. It may also result in more appropriate utilization of medical imaging (potentially having associated health risks) and reductions in hospitalizations. Patients discharged from the ED who were deemed to not require a CT scan will be followed-up for outcome.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
EEG recording acquired on BrainScope One device.
Cognitive performance tests performed on BrainScope One device.
Clinician evaluation performed as part of standard of care at the clinical site.
Self assessed 22-item Concussion Symptom Inventory (CSI).
Time frame: 30 days
Demonstrate the accuracy of the BrainScope Structural Injury Classifier (SIC) negative findings through repeated follow ups of those patients discharged from the ED without receiving a CT scan, as determined by the ED physician.
Time frame: After enrollment closure
For those who were BSC SIC negative and who are referred to CT due to clinician's decision, CT results will be obtained to assess the accuracy of BrainScope finding, this will allow an estimate of NPV.
Time frame: After enrollment closure
Compare accuracy of Nexus II and CCHR Imaging rules to BrainScope in predicting true negatives
Time frame: After enrollment closure
The BFI/CI can help to inform the clinical decision on the likely of concussion at the time of injury in the ED environment and predict prolonged recovery.
BrainScope Company, Inc.
Industry
Acronym: MEDO
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06494592
Brain Concussion, Brain Diseases
Boston, Massachusetts, United States
View Trial DetailsNCT04776304
Anger, Brain Concussion
Bethesda, Maryland, United States
View Trial DetailsNCT04121780
Anterior Pituitary Hyposecretion Syndrome, Bone Diseases
Dearborn, Michigan, United States
View Trial DetailsNCT04095377
ABD, ADHD
Rishon LeZiyyon, Israel
View Trial Details