Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
1200

Summary

Conditions
  • Critical Illness
  • Oxygen Toxicity
  • Trauma
Design
Observational Model: Case-ControlTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 109 years
Gender
Both males and females

Description

Supplemental oxygen is fundamental in caring for critically ill trauma. While the avoidance of hypoxia is vital, the current clinical practice of excessive oxygenation settings is common, and unnecessary, and may even be harmful. An expert panel convened to define optimal oxygenation targets in crit...

Supplemental oxygen is fundamental in caring for critically ill trauma. While the avoidance of hypoxia is vital, the current clinical practice of excessive oxygenation settings is common, and unnecessary, and may even be harmful. An expert panel convened to define optimal oxygenation targets in critically ill trauma patients. The strong consensus was to target normoxia at an oxygen saturation (SpO2) range of 90-96% and arterial oxygen (PaO2) range of 60-100 mmHg. Accordingly, a pilot trial implementation of this consensus will occur for the care of trauma patients. Specific Aim: This is an observational pre/post study to evaluate the impact of targeted normoxia implementation in optimizing oxygen delivery and oxygenation in critically ill trauma patients. Hypotheses: That the clinical efforts to improve adherence to oxygen guidelines will: improve the proportion of time spent with target normoxia thresholds (oxygen saturation SpO2 90-96%) by reducing utilization of unnecessary supplementation oxygen without a substantive increase in hypoxic episodes or an adverse impact on clinical outcomes.

Tracking Information

NCT #
NCT03789396
Collaborators
United States Department of Defense
Investigators
Principal Investigator: Adit Ginde, MD, MPH University of Colorado, Denver