RecruitingNCT04565119

Biomarkers in the Brain Oxygen Optimization in Severe Traumatic Brain Injury Trial

Biomarkers in the Brain Oxygen Optimization in Severe Traumatic Brain Injury Trial (BioBOOST)


Sponsor

University of Pennsylvania

Enrollment

300 participants

Start Date

Dec 20, 2020

Study Type

OBSERVATIONAL

Conditions

Summary

BioBOOST is a multicenter, observational study of the effect of derangements in brain physiologic parameters on brain injury biomarker levels in patients with severe traumatic brain injury.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Enrolled in BOOST-3 (this is an ancillary study to the BOOST-3 trial)
  • BOOST-3 participant is enrolled at a BioBOOST site
  • Able to maintain initial blood sample within 24 hours of injury
  • Provide proxy informed consent

Exclusion Criteria2

  • Profoundly anemic (subjects who are profoundly anemic require blood transfusion)
  • Age less than 18 years

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Interventions

OTHERNo intervention. This is an observational study.

There are no interventions being tested in the Bio-BOOST study.


Locations(2)

University of Michigan

Ann Arbor, Michigan, United States

Penn Presbyterian Medical Center

Philadelphia, Pennsylvania, United States

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NCT04565119


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