Actively Recruiting
Reproducibility, Intra- and Inter-Observer Variability of Bedside Cardiac Ultrasound Measurements in Healthy Volunteers
Led by Medical University of Warsaw · Updated on 2026-05-22
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research evaluates the use of transthoracic echocardiography to measure Left Ventricular Outflow Tract Velocity-Time Integral (LVOT VTI) in healthy volunteers. LVOT VTI is a key ultrasound measurement that helps estimate important heart function parameters like stroke volume and cardiac output. The study aims to compare measurements taken by minimally trained operators with those by expert clinicians to understand measurement consistency and variability. Operators, including medical students and licensed physicians with minimal training, will perform echocardiography to measure LVOT VTI on healthy participants. The study focuses on assessing how closely these novice measurements match those by experienced operators, as well as evaluating differences between and within operators. All measurements and assessments take place on the same day, with time needed for each measurement also recorded. Participants will undergo a single evaluation where novice operators measure LVOT VTI after brief training, and their results will be compared with those from an expert operator. Researchers will assess agreement between measurements, variability among operators, and time to complete measurements. The study is observational and involves healthy adult volunteers aged 18 years or older, with no prior cardiac ultrasound experience allowed for operators.
CONDITIONS
Brief Title
Assessment of LVOT VTI in Healthy Volunteers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 18 years
- Medical student at Medical University of Warsaw or licensed physician
You will not qualify if you...
- Age < 18 years
- Prior experience in performing cardiac ultrasound examinations, including apical five- and three-chamber views and Doppler measurements of LVOT VTI
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 2 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants undergo transthoracic echocardiography performed by operators with minimal training to measure LVOT VTI and compare with measurements from experienced operators.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Medical University of Warsaw
Warsaw, Poland
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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