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Assessment of Head Injury in the Emergency Department Using BrainScope® Ahead® Technology

NCT01556711 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 816

Last updated 2013-12-10

No results posted yet for this study

Summary

The objectives of the study are to document device performance with respect to the primary and secondary endpoints.

Conditions

  • Brain Injuries
  • Craniocerebral Trauma

Sponsors & Collaborators

  • BrainScope Company, Inc.

    lead INDUSTRY

Principal Investigators

  • Robert A De Lorenzo, MD · Brooke Army Medical Center

  • Peter Cuenca, MD · Brooke Army Medical Center

  • Samuel M Galvagno, DO · University of Maryland R. Cowley Shock Trauma Center

  • Stephen J Huff, MD · University of Virginia Medical Center

  • Rosanne Naunheim, MD · Washington University - Barnes Jewish Hospital

  • Brian O'Neil, MD · Wayne State University - Detroit Receiving Hospital

  • Brian J O'Neil, MD · Wayne State University - Sinai Grace Hospital

  • Sandeep Johar, DO · Hartford Hospital

  • Bradley Kolls, MD · Duke University Medical Cetner

  • Jeffrey Bazarian, MD · University of Rochester

  • James Ecklund, MD · Inova Fairfax Hospital

  • Kevin Crutchfield, MD · Sinai Hospital

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01556711 on ClinicalTrials.gov