Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside V… (NCT07541768) | Clinical Trial Compass
RecruitingNot Applicable
Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment.
Switzerland23 participantsStarted 2026-03-20
Plain-language 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.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial seems to be focused on training residents to use a specific ultrasound technique called VExUS to assess fluid overload — does that mean I would primarily be helping train doctors rather than receiving an experimental treatment myself, and how would that affect my care?
2Since the main thing being measured is the quality of ultrasound images taken by residents-in-training, would my diagnosis and treatment decisions be guided by these trainee assessments, and would an experienced physician also be reviewing my results independently?
3I have acute heart failure with fluid congestion — would my doctor consider this trial a good fit for my current condition, or would standard approaches to managing my fluid levels be a better first step before involving a training program?
4Since this trial has no assigned phase (listed as 'NA'), which usually means it's more of an educational or feasibility study rather than a drug or device test, can my doctor explain exactly what risks or benefits I should realistically expect from participating?
5If a resident's VExUS ultrasound assessment of my venous congestion turns out to be inaccurate during the training process, what safeguards are in place to make sure my treatment plan isn't negatively affected?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Ultrasound Image Quality Score
Timeframe: From training until 6 months after completion of training