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Recruiting Not applicable NCT07541768

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

No applicable phase (e.g. observational)
Conditions: Acute Heart Failure (AHF) Fluid Over-load Congestion Congestion, Venous

Sponsor: Insel Gruppe AG, University Hospital Bern

trial.available_in: БГ
Overview
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.
Description
Accurate assessment of volume status is essential in managing acute heart failure but remains challenging in clinical practice. The VExUS score is a validated ultrasound-based tool integrating inferior vena cava diameter and Doppler assessment of hepatic, portal, and intrarenal veins. This single-center randomized controlled trial compares two training modalities (in-person vs. remote) in medical residents with basic ultrasound skills. Participants will be randomized 1:1 to either training method and compared to a control group of expert physicians. Primary outcomes include ultrasound image quality assessed using a standardized 100-point score. Secondary outcomes include time to acquisition, VExUS scoring accuracy, self-confidence, and acceptability of training methods.
Who can participate
Inclusion Criteria: * Medical residents in general internal medicine * Basic ultrasound skills (POCUS component 1 or ≥200 scans) * Working at study site during study period Exclusion Criteria: * SGUM certification in abdominal ultrasound * Advanced duplex ultrasound experience * Prior vascular/duplex training
Interventions
In-person VExUS Training Program
BEHAVIORAL
Remote VExUS Training Program
BEHAVIORAL
No intervention
OTHER
Locations 1
Switzerland (1)
Inselspital
Bern
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Healthy volunteers
No
Start date
20.03.2026
Completion date
31.12.2026
Registry ID
NCT07541768
Source
clinicaltrials.gov
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