Traumatic Brain Injury Clinical Trial
Official title:
Accuracy of S-100B as Pre-Head CT Scan Screening Test After Mild Traumatic Brain Injury
Verified date | June 2015 |
Source | University of Rochester |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The purpose of the study is to determine if a specific blood protein, S-100B, can help predict who will have a traumatic abnormality on head CT scan after a concussion. We will compare the levels of this protein in the subject's blood to the initial head CT scan and to how the subject is feeling one month after injury. We hope that the information we collect in this trial will help us determine who needs a head CT scan after a concussion and who may be more likely to have trouble recovering from a concussion.
Status | Completed |
Enrollment | 1252 |
Est. completion date | September 2010 |
Est. primary completion date | September 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Patients presenting with head trauma to any of the AHCC/ERNES EDs, meeting the following criteria will be eligible to participate: - Presence of mild TBI per study definition - Arrival at the ED within 4 hours of injury - ED workup includes a Head CT (Controls are eligible if they present to the Outpatient Lab for routine bloodwork during enrollment hours) Exclusion Criteria: - Time of injury not able to be determined - Head CT not done as part of clinical emergency care - Incarcerated - Non-English or Spanish speakers - Absence of parent/guardian for minor subjects - Subject and/or parent/guardian do not have capacity to consent - Head injury due to birth trauma, anoxia, inflammatory, toxic, infectious or metabolic encephalopathies that are not complications of head trauma - Ischemic or hemorrhagic stroke without associated trauma (Controls are excluded if they have any of the following:History of brain tumor, melanoma and/or Alzheimer's disease; History of concussion, bone fracture or stroke (CVA or TIA) in the past month; History of surgery in the past month; Inability to obtain consent from subject and/or parent due to lack of capacity or absence of parent/guardian of minor; Inability to speak or read English; Incarceration) |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Albany Medical College | Albany | New York |
United States | Erie County Medical Center | Buffalo | New York |
United States | Bassett Healthcare | Cooperstown | New York |
United States | University of Rochester Medical Center | Rochester | New York |
United States | Guthrie | Sayre | Pennsylvania |
United States | SUNY Upstate Medical Center at Syracuse | Syracuse | New York |
Lead Sponsor | Collaborator |
---|---|
University of Rochester | Academic Health Center Consortium (not Univ of Minnesota), Emergency Research Network of the Empire State, New York State Department of Health |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Head CT scan | At time of injury in ED | No | |
Secondary | Post concussive symptoms | One month after injury | No |
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