Clinical Trials Directory

Trials / Completed

CompletedNCT03225378

Changes in PPV Induced by PLR Test to Predict Fluid Responsiveness in ICU

Changes in Pulse Pressure Variations Induced by Passive Leg Raising Test to Predict Fluid Responsiveness in ICU

Status
Completed
Phase
Study type
Observational
Enrollment
286 (actual)
Sponsor
Centre Hospitalier Arras · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERFluid loading of 500 mL of crystalloid solutionInfusion of 500 mL of crystalloid solution in less than 15 minutes
OTHERPassive Leg Raising testThis intervention is done before the fluid loading in order to predict fluid responsiveness.

Timeline

Start date
2017-09-21
Primary completion
2021-09-20
Completion
2021-09-20
First posted
2017-07-21
Last updated
2021-10-27

Locations

12 sites across 1 country: France

Source: ClinicalTrials.gov record NCT03225378. Inclusion in this directory is not an endorsement.