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Fresh Intravenous Blood Samples for TBI Diagnostic Assay Development With Philips Point of Care System

NCT03060109 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 317

Last updated 2017-10-02

No results posted yet for this study

Summary

The purpose of this study is to collect fresh whole blood within 12 hours from suspected mild head injury (Glasgow Coma Scale score 13-15) from subjects over the age of 18, to help verify that both UCH-L1 and GFAP can be detected with the Philips Minicare POC diagnostic test platform.

Conditions

Interventions

OTHER

Blood draw within 12 hours of injury

Sponsors & Collaborators

  • U.S. Army Medical Research and Development Command

    collaborator FED

  • Banyan Biomarkers, Inc

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-21
Primary Completion
2017-09-10
Completion
2017-09-10

Countries

  • Netherlands

Study Locations

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Entities

Diseases

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 NCT03060109 on ClinicalTrials.gov