Clinical Trials Logo

Clinical Trial Summary

Acute circulatory failure (ACF) is a common cause of admission in intensive care unit (ICU). Echocardiography is a widespread tool nowadays for the initial assessment and the hemodynamic monitoring. An interesting data from this exam is the Left ventricular outflow tract (LVOT) velocity time integral (VTI), reflecting stroke volume, and therefore cardiac output. A new tool for automated recording has been developped on the VENUE GE echograph. This study aims at assessing this automated measurement of LVOT VTI compared with the classic manual method.


Clinical Trial Description

Acute circulatory failure is a dramatically common issue in critical care, affecting nearly 1/3 of the patients admitted in ICU, and associated with a high morbi-mortality. Echocardiography enables a quick point of care assessment of the hemodynamic status of the patient. One key parameter is stroke volume, which can be estimated by LVOT VTI. In practice, the guidelines recommend measuring LVOT VTI in a 5 chambers cavity window with pulsed wave doppler, trying to get an angle between aortic flow and the doppler signal as cloth as possible to 0°. Than VTI must be calculated from an average of 3 to 5 cycles in sinus rhythm, or 5 to 10 cycles in arrythmia such as atrial fibrillation. The main issue is that this approach is time consuming and tedious, and most of the practitioners choose to measure only the most representative beat (" Best VTI "), likely to be source of a loss of reproducibility. In order to make it easier, some companies have developed softwares to help the intensivist. Thereby, General Electric has equiped the VENUE echograph with a system that helps first selecting the proper place for sampling, and then automatically acquire, trace, and calculate the average LVOT VTI based on a 4 seconds sample. Finally, this tool gives a VTI trending when several measures are repeated along the patient' stay. This program has already been tested on a swine model in hemorrhagic shock with encouraging results (better agreement with cardiac output by thermodilution with the automated method than with the manual one). However, feasibility was only 60%. This human study aims at assessing the interest of automated LVOT VTI measurement compared to the manual standard one when performing a cardiac echography for hemodynamic assessment of patients hospitalised in ICU. Otherwise, a measure of the " Best-VTI " will be done at the same time in accordance with the current practice, in order to assess this approach. Finally, when a fluid resuscitation will be indicated, a second exam will be done, and agreement of VTI variation between automated and manual method studied. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04360304
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Completed
Phase N/A
Start date January 29, 2020
Completion date October 21, 2020

See also
  Status Clinical Trial Phase
Completed NCT03225378 - Changes in PPV Induced by PLR Test to Predict Fluid Responsiveness in ICU
Completed NCT03680963 - Early Versus Differed Arterial Catheterization in Critically Ill Patients With Acute Circulatory Failure: N/A
Terminated NCT01090791 - FLOTRAC/VIGILEO in Acute Circulatory Failure N/A
Completed NCT04337983 - Hemodynamic Characteristics of Patients With SARS-CoV-2
Recruiting NCT04946643 - Subclavian Vein Diameter Variations to Assess Vascular Filling
Recruiting NCT03788772 - Systems Analysis of Antigen Presenting Cells in Human Sepsis N/A
Completed NCT02050269 - Measuring the Plasma Clearance of Iohexol to Estimate Glomerular Filtration Rate in Intensive Care Unit Patients: Preliminary Feasibility Study Phase 3
Completed NCT01630577 - Central Venous Pressure Change With Volume Challenge in Patients With Hemodynamic Instability Phase 3
Recruiting NCT05046340 - Applicability of Fluid Responsiveness Indices in Circulatory Failure (AFRIC Study) Study Project
Completed NCT04250389 - Microcirculatory Effects of Methylene Blue
Recruiting NCT05613647 - Concordance Study of Therapeutic Decision-making in Patients With Shock Based on Hemodynamic Monitoring
Completed NCT05847998 - Second Generation DICART Prototype Validation N/A
Not yet recruiting NCT06384287 - Peripheral Tissue Perfusion in Intensive Care
Recruiting NCT02878369 - Evaluation of Doppler Flow From the Femoral Artery as a Reflection of Cardiac Flow in a Vascular Fluid Test N/A
Completed NCT03694717 - Time Course Evolution of Cardiac Output