Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Bedside point-of-care ultrasound to improve diagnosis of chest and belly pain in the emergency department

Official title: PoCUS Impact on the Diagnostic Approach for Thoracic and Abdominal Pain in the ED

Run by Cliniques universitaires Saint-Luc- Université Catholique de Louvain · NCT06827730 · Data updated 2026-11-12

This will test whether point-of-care (bedside) ultrasound helps doctors make better diagnostic and management decisions for adults who come to the emergency department with chest or abdominal pain.

More Abdominal Pain trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment406 (estimated)
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain
Academic / other
Locations1 site (Brussels)
StatusRecruiting
StartedJune 1, 2025
Main results expectedJune 1, 2028
Study endsJune 1, 2029
Registry record updatedApril 30, 2026
Trial IDNCT06827730 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults older than 17 who present to a participating ED within 72 hours of thoracic or abdominal pain, can provide informed consent, and can complete one-month follow-up are ideal candidates.

Probably not a fit

Patients who are found to be pregnant during emergency care, those with reasons that make abdominal ultrasound impossible, or those who cannot be followed up at one month are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter prospective interventional protocol enrolls adults presenting to participating emergency departments with thoracic or abdominal pain of less than 72 hours. Clinicians will perform point-of-care ultrasound as part of the clinical exam, and an independent adjudication committee of three blinded reviewers will compare diagnostic choices and planned management with and without the PoCUS information. The study focuses on how PoCUS changes the diagnostic approach, including differential diagnoses, treatment selection, and additional tests ordered. Patients with technical barriers to ultrasound, newly discovered pregnancy, or inability to complete one-month follow-up are excluded.

Why it matters

Potential benefit: If successful, PoCUS could speed more accurate bedside decision-making, leading to faster appropriate treatment and fewer unnecessary tests for people with chest or belly pain.

How similar studies have gone: Prior research shows PoCUS improves detection of specific conditions (for example free fluid, pneumothorax, or biliary disease) and can speed decision-making, but few multicenter prospective trials have measured its effect on the overall diagnostic strategy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* \> 17 years
* Thoracic or abdominal pain for less than 72 hours
* Signed informed consent

Exclusion Criteria:

* Reasons making abdominal ultrasound impossible
* Discovery of a pregnancy during emergency care
* Follow-up impossible at one month

Where it's running

  • Cliniques universitaires Saint Luc
    Brussels, Belgium
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.