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Clinical Trial Summary

This study uses the portal vein pulsatility index (PVPI) to assess fluid intolerance amongst fluid responders.


Clinical Trial Description

This prospective observational study aims to use the portal vein pulsatility index (PVPI) to assess fluid intolerance in fluid responders. The investigators will enroll mechanically ventilated postoperative adult patients within 6 hours of ICU admission after cardiac surgery. Patients will undergo a Passive Leg Raising (PLR) test and Left Ventricular Outflow Tract (LVOT) recording using transthoracic echocardiography. The main objective is to predict fluid intolerance after a fluid challenge of 7 ml/kg Ringer Lactate over 10 minutes in initially tolerant fluid responders. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06440772
Study type Observational
Source Institutul de Urgenta pentru Boli Cardiovasculare Prof.Dr. C.C. Iliescu
Contact Cosmin Balan, PhD
Phone +40722751501
Email cosmin13mara@yahoo.com
Status Recruiting
Phase
Start date July 1, 2023
Completion date July 1, 2024

See also
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Completed NCT05828407 - Fluid Challenge Impact in the Portal Vein Pulsatility Depending on the Fluid Responsivness Status
Recruiting NCT06251713 - Fluid-removal Guided by VeXUS Score With Usual Care in Patients With Acute Kidney Injury After Cardiac Surgery N/A
Recruiting NCT04914455 - Transhepatic Echography for Fluid Responsiveness After Cardiovascular Surgery
Not yet recruiting NCT06160856 - Correlation of Ultrasonography Indices of Venous Congestion With Intra-abdominal Pressure in ICU Patients.