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Pilot Study to Measure Uric Acid in Traumatized Patients: Determinants and Prognostic Association

M

Montreal Sacred Heart Hospital

Status

Unknown

Conditions

Inflammation
Trauma

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this project, is to better understand the fluctuation of the level of uric acid in traumatized patients by making serial measurements during their hospitalization in the intensive care unit. In addition, the determinants (e.g. type of trauma, diseases, interventions) of the blood level of uric acid and its association with the development of organ failure will be sought.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Direct admission to trauma center
  • ≤ 3h after trauma
  • ISS ≥ 16
  • Received at least 1L of fluid at ER entrance

Exclusion criteria

  • Isolated head injury
  • Isolated spine injury
  • Chemotherapy within the last month
  • Hematologic disease
  • Chronic hemodialysis
  • Uricase treatment within the last week
  • Expected death within 48h

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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