Transthoracic echocardiography: an accurate and precise method for estimating cardiac output in the critically ill patient.
Pablo Mercado, Julien Maizel, Christophe Beyls...
https://pubmed.ncbi.nlm.nih.gov/28595621/Actively Recruiting
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-04-21
100
Participants Needed
3
Research Sites
N/A
Total Duration
Researchers are studying the reliability of measuring stroke volume in critically ill patients with unstable blood flow and low tissue oxygen levels. The study focuses on comparing measurements of Left Ventricular Outflow Tract LVOT Velocity-Time Integral VTI, an important ultrasound estimate of stroke volume, between minimally trained operators and expert intensive care physicians. This research evaluates the use of UltraSight AI software to guide operators in obtaining accurate heart images, aiming to improve basic ultrasound skills in intensive care. The trial involves two groups minimally trained operators, including intensive care residents and medical students with limited ultrasound experience, and expert ICU physicians. Both groups use the same ultrasound device equipped with AI guidance to capture heart images and measure LVOT VTI. Patients needing fluid administration due to low tissue perfusion will undergo a fluid challenge or passive leg raising test, with LVOT VTI measured before and after by both operator groups independently and blinded to each other. Participants will have their LVOT VTI measured by both operator types within 60 minutes, assessing the difference and agreement between measurements. Researchers will also evaluate how these measurements influence therapeutic decisions regarding fluid administration. The study includes monitoring of various measurement differences and correlations to confirm if minimally trained operators can reliably perform these critical assessments using AI guidance.
CONDITIONS
Reliability of Minimally Trained Operator's Velocity-Time Integral Measurement Guided by Artificial Intelligence VTI
B
Bernard Cholley
C
Cléo Bourgeois
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Assistance Publique - Hôpitaux de Paris
Lead Sponsor
Philips Healthcare
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Less than 60 minutes
Participants undergo LVOT VTI measurements by both minimally trained and expert operators guided by AI software, before and after a fluid challenge or passive leg raising test.
1 visit (in-person)
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
2
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Lead Sponsor
Philips Healthcare
Collaborating Sponsor