Creating a tool to improve CT imaging decisions for blunt trauma patients
Developing a Decision Instrument to Guide Abdominal-pelvic CT Imaging of Blunt Trauma Patients
This study is testing a new tool to help doctors decide when CT scans are really needed for patients with blunt trauma to avoid unnecessary radiation and costs.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 12000 (estimated) |
| Sex | All |
| Sponsor | University of California, Los Angeles Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (Los Angeles, California) |
| Trial ID | NCT04937868 on ClinicalTrials.gov |
What this trial studies
This observational study aims to develop a decision instrument that will help clinicians determine when abdominal-pelvic CT imaging is necessary for patients with blunt trauma. The study addresses the issue of overuse of CT scans, which can expose patients to unnecessary radiation and high costs without significantly improving outcomes. By identifying 'low risk' patients who do not require imaging, the study seeks to enhance clinical decision-making and reduce healthcare expenses. The research will analyze existing criteria to establish reliable guidelines for selective imaging in trauma cases.
Who should consider this trial
Good fit: Ideal candidates for this study are blunt trauma patients who are undergoing abdominal-pelvic CT imaging in the emergency department.
Not a fit: Patients who do not undergo abdominal-pelvic CT imaging or those with non-blunt trauma injuries may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce unnecessary radiation exposure and healthcare costs for blunt trauma patients.
How similar studies have performed: Other studies have indicated that selective imaging approaches can improve patient outcomes and reduce unnecessary procedures, suggesting that this study's approach is promising.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Blunt trauma patients who undergo abdominal-pelvic CT imaging during their initial trauma evaluation in the emergency department. Exclusion Criteria: None
Where this trial is running
Los Angeles, California
- Ronald Reagan Hospital — Los Angeles, California, United States (Recruiting)
Study contacts
- Study coordinator: William R Mower, MD, PhD
- Email: wmower@ucla.edu
- Phone: (310) 794-0599
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.