Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06827730

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age greater than 17 years
  • Thoracic or abdominal pain for less than 72 hours
  • Signed informed consent
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Cliniques universitaires Saint Luc

Brussels, Belgium, 1200

Actively Recruiting

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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

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