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Changes in Pulse Pressure Variations Induced by Passive Leg Raising Test to Predict Fluid Responsiveness in ICU
The passive leg raising (PLR) test is a reversible preload challenge of around 300 mL of blood that can be repeated as frequently as required without infusing a drop of fluid. Two recent meta-analyses of many studies have confirmed the reliability of the PLR test to predict fluid responsiveness in patients with acute circulatory failure. Nevertheless, the effects of the PLR must be assessed by the direct measurement of cardiac output since changes in arterial pressure do not allow the assessment of the PLR hemodynamic effects with reliability. Moreover, cardiac output must be measured continuously and in real time. In clinical practice, cardiac output measurement can be difficult for different reasons such as the unavailability of the echocardiography machine, or the absence of any continuous cardiac output monitoring technique at the time of acute circulatory failure occurrence. Recently, it was shown that the decrease in pulse pressure variation (PPV) induced by the mini-fluid challenge (100 mL of colloid solution infused in 1 min) was able to predict fluid responsiveness with reliability in patients ventilated with low tidal volume (\<8 mL/kg of ideal body weight). Therefore, the investigators hypothesize that the changes in PPV induced by PLR test could be able to predict fluid responsiveness with reliability in mechanically ventilated patients with acute circulatory failure.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
CHU d'Amiens - Réanimation Cardio-Thoracique-Vasculaire
Amiens, France
CHU d'Amiens - Réanimation chirurgicale
Amiens, France
Centre Hospitalier d'Arras
Arras, France
Centre Hospitalier de Béthune
Béthune, France
CH Boulogne-sur-mer
Boulogne-sur-Mer, France
CHU de Caen
Caen, France
Centre Hospitalier de Cambrai
Cambrai, France
CHU de Dijon
Dijon, France
Centre Hospitalier de Lens - Anesthésie-Réanimation
Lens, France
Centre Hospitalier de Lens - Réanimation
Lens, France
Start Date
September 21, 2017
Primary Completion Date
September 20, 2021
Completion Date
September 20, 2021
Last Updated
October 27, 2021
286
ACTUAL participants
Fluid loading of 500 mL of crystalloid solution
OTHER
Passive Leg Raising test
OTHER
Lead Sponsor
Centre Hospitalier Arras
NCT04360304
NCT02858115
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT01630577