Actively Recruiting
PoCUS Impact on the Diagnostic Approach for Thoracic and Abdominal Pain in the ED
Led by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · Updated on 2026-04-30
406
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
Sponsors
C
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead Sponsor
A
APHP
Collaborating Sponsor
AI-Summary
What this Trial Is About
Many medical specialties and paramedical fields are increasingly using point-of-care ultrasound (PoCUS). In daily practice, thoracic and abdominal pain constitute a significant portion of emergency department consultations. PoCUS can be employed in various ways during thoracic and abdominal physical examinations. Most scientific societies advocate for its use to address specific clinical questions rather than to provide a definitive diagnosis. The integration of PoCUS into clinical examinations raises the question of its effectiveness in improving the diagnostic approach, rather than its diagnostic accuracy alone. Given the broad spectrum of differential diagnoses for thoracic and abdominal pain, this multicenter prospective study protocol aims to evaluate how PoCUS enhances the diagnostic approach for patients presenting with these symptoms in the emergency department. To assess the contribution of PoCUS, three members of an adjudication committee will blindly choose between two case report forms reporting the planned diagnostic approach for each patient: one completed before PoCUS and the other after its use by the investigator handling the case. The hypothesis that PoCUS improves the diagnostic approach by 60% will be reached if 60% of the improved diagnostic approaches favor the case report form filled out after PoCUS.
CONDITIONS
Official Title
PoCUS Impact on the Diagnostic Approach for Thoracic and Abdominal Pain in the ED
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age greater than 17 years
- Thoracic or abdominal pain for less than 72 hours
- Signed informed consent
You will not qualify if you...
- Conditions that make abdominal ultrasound impossible
- Pregnancy discovered during emergency care
- Unable to complete one-month follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cliniques universitaires Saint Luc
Brussels, Belgium, 1200
Actively Recruiting
Research Team
F
Florence MV Dupriez, MD, PhD
CONTACT
L
Lara Absil, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here