N/A
N=182
A Study to Improve the FAST Ultrasound Exam
Hemoperitoneum
Bottom Line
View on ClinicalTrials.gov: NCT02991521 ↗Enrolled (actual)
182
Serious AEs
0.0%
Results posted
Mar 2024
Primary outcome: Primary: Number of Subjects Screening Positive for Blood Around the Abdominal Organs (Hemoperitoneum) After Trauma, as Assessed by Focused Assessment With Sonography for Trauma (FAST), a Rapid Bedside Ultrasound Examination. — 65 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Fast exam (Procedure)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- The Guthrie Clinic
- Primary completion
- Jun 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Subjects Screening Positive for Blood Around the Abdominal Organs (Hemoperitoneum) After Trauma, as Assessed by Focused Assessment With Sonography for Trauma (FAST), a Rapid Bedside Ultrasound Examination. |
65 | — |
Summary
This research study aims to improve the standard exam called Focused Assessment with Sonography in Trauma (FAST). The FAST exam is an ultrasound test used to identify an abdominal bleed. The study will see if having patients roll on their right side improves the FAST exam. Making the FAST exam better can help trauma doctors save the lives of patients with bleeding.
Eligibility Criteria
Inclusion Criteria
- All trauma patients who present as a Trauma Activation with clinical history or physical signs of blunt abdominal trauma.
Exclusion Criteria
- Pregnant females
- Prisoners
- Patients with prohibitive right sided chest trauma
- Patients in extremis undergoing salvage maneuvers (chest compressions or emergent surgical intervention) which prevents performance of an ultrasound examination
- Patient who leave against medical advice or are otherwise removed from the medical system before their work up has been completed
Data sourced from ClinicalTrials.gov (NCT02991521). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.