Strategy to Avoid Excessive Oxygen for Critically Ill Trauma Patients
Running, not enrolling · Phase 3
Conditions studied: Critical Illness, Wounds and Injury, Disease Attributes, Pathologic Processes
In brief
The objective is to determine the effectiveness of a multimodal educational intervention to reduce supplemental oxygen use in critically injured patients. Investigators will also evaluate the safety and clinical effectiveness of the more targeted use of oxygen therapy.
Key facts
- Study ID
- NCT04534959
- Run by
- University of Colorado, Denver
- People needed
- 6000
- Starts
- 2020-10-15
- Expected to finish
- 2025-06-30
- Last updated by the study team
- 2025-04-02
Who can join
Age: 18 and older, up to 120. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Acutely injured patients who meet the criteria for entry into the state or national trauma registry
- Admission to surgical/trauma ICU within 24 hours of hospital arrival
You may not qualify if…
- Age <18 years
- Prisoners
- Known pregnancy
- Transferred patients not admitted through the emergency department
Where it is running
- University of Alabama-Birmingham Medical Center — Birmingham, Alabama, United States
- Denver Health — Denver, Colorado, United States
- University of Cincinnati Medical Center — Cincinnati, Ohio, United States
- Oregon Health and Sciences University — Portland, Oregon, United States
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
- Brooke Army Medical Center — Fort Sam Houston, Texas, United States
- The University of Texas Health Science Center at Houston — Houston, Texas, United States
Full record on ClinicalTrials.gov
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