RecruitingNot ApplicableNCT07541768

Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment.

Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment: a Randomized Controlled Trial


Sponsor

Insel Gruppe AG, University Hospital Bern

Enrollment

23 participants

Start Date

Mar 20, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This randomized controlled trial evaluates the effectiveness of two training approaches (in-person versus remote) for teaching medical residents to apply the Venous Excess Ultrasound (VExUS) score for bedside volume assessment in patients with acute heart failure. Resident performance will be compared to that of expert physicians certified in abdominal and duplex sonography.


Eligibility

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a behavioral approach called In-person VExUS Training Program, No intervention, and others for people with acute heart failure (ahf), congestion, and other related conditions. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALIn-person VExUS Training Program

In-person training consisting of a 1-hour theoretical introduction followed by a 3-hour supervised hands-on ultrasound training session focusing on acquisition and interpretation of the VExUS score.

BEHAVIORALRemote VExUS Training Program

Remote training consisting of an e-learning module followed by independently performed ultrasound examinations with asynchronous expert feedback (via phone or email).

OTHERNo intervention

SGUM-certified physicians performing VExUS examinations as expert reference standard.


Locations(1)

Inselspital

Bern, Switzerland

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NCT07541768


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