Actively Recruiting
Point-of-care Ultrasound in the Assessment of Snake Bite
Led by University of Arizona · Updated on 2025-04-18
150
Participants Needed
1
Research Sites
370 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Early identification of tissue injury from a rattlesnake bite is critical to prevent complications and reduce health care costs. Given the limitations of clinical assessment, there is a need to develop a more objective reproducible, anatomically detailed diagnostic tool for to accurately assess tissue damage and assist with timely administration of antivenom, if needed. Emergency physician performed point-of-care ultrasonography has been shown to be beneficial in the diagnosis and management of skin and soft tissue infections. The innovative use of bedside ultrasound technology can provide new information to individualize antivenom treatment and to improve patient outcomes. The objectives of this study is to compare clinical assessment and bedside ultrasound findings in the detection of tissue injury in emergency department patients with rattle snakebite and determine if bedside ultrasound can alter management (antivenom dosing) in emergency department patients with rattle snakebite.
CONDITIONS
Official Title
Point-of-care Ultrasound in the Assessment of Snake Bite
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients (18 years and older)
- Both genders
- Complaint of snake bite
You will not qualify if you...
- Unwilling to provide informed consent
- Hemodynamically unstable patients (shock, respiratory distress, altered mental status, or cardiorespiratory arrest)
- Vulnerable populations: children, pregnant patients, prisoners, and patients unable to verbally consent due to cognitive impairment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Banner University Medical Center-Tucson
Tucson, Arizona, United States, 85724
Actively Recruiting
Research Team
S
Srikar Adhikari, MD, MS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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