RApid Fluid Volume EXpansion in Patients in Shock After the Initial Phase of Resuscitation.
NCT02645851 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 98
Last updated 2025-02-14
Summary
Rapid volume expansion using repeated intravenous fluid boluses is a very common intervention performed in the intensive care unit (ICU) in the early days of resuscitation of patients with shock. Once passed the initial phase of resuscitation, the fluid boluses administered fail to effectively increase the patients' cardiac output in about 50% of cases. Pulse pressure changes or stroke volume changes induced by a Passive Leg Raising (PLR) test have acceptable/good ability to predict fluid responsiveness (in terms of cardiac output change) and may be systematically used in patients with persistent shock with the aim of limiting the total amount of fluid administered to patients by avoiding undue fluid boluses. One may suppose that such a volume expansion management policy could impact morbidity and mortality of shocked patients. Among the predictive indices available in clinical practice, the PLR test has the advantages of being usable regardless of the patients' respiratory status and cardiac rhythm. Changes in left ventricular stroke volume during the PLR test perform better that changes in pulse pressure to predict fluid responsiveness. However, in counterpart, pulse pressure changes during PLR can be assessed without the need of other hemodynamic exploration such central venous pressure measurement or cardiac output monitoring. The investigators hypothesized that strategies using either stroke volume changes or pulse pressure changes induced by the PLR test to decide wether a fluid bolus clinically deemed indicated should or should not be administered, may limit the amount of fluid received by the patients during the first 5 days of shock, improve their oxygenation index, and shorten the time passed under mechanical ventilation, as compared to a "liberal" strategy (usual care) that does not use predictive indices of fluid responsiveness.
Conditions
- Shock
- Hypovolemia
Interventions
- DRUG
-
fluid bolus
Administration of the fluid bolus if deemed clinically necessary, OR if deemed clinically necessary AND PLR-induced SV or PP changes ≥10%, depending of the Arm the patient is assigned to
- DEVICE
-
PiCCO system (Pulsion, Germany)
During the intervention period (from inclusion to the 120th hour), every time a fluid bolus is deemed necessary, fluid responsiveness will be assessed by Stroke Volume changes obtained at 1 min of a Passive Leg Raising (PLR) test (fluid will be given if PLR-induced stroke volume change is over 10%; in case stroke volume change is below 10%, fluid will not be given and need for fluid reassessed after a short period of time, as in usual care)
- DEVICE
-
Vascular pressure transducers (Edwards Life Science, USA)
During the intervention period (from inclusion to the 120th hour), every time a fluid bolus is deemed necessary, fluid responsiveness will be assessed by Pulse Pressure changes obtained at 1 min of a Passive Leg Raising (PLR) test (fluid will be given if PLR-induced Pulse Pressure change is over 10%; in case Pulse Pressure change is below 10%, fluid will not be given and need for fluid reassessed after a short period of time, as in usual care)
- OTHER
-
Passive Leg Raising test
Passive elevation of the legs of the patient, and lying down of the trunk (if patient is in the semi-recumbent position), preferably using electric bed. If not available, elevation of the legs by an assistant to a 45 degrees angle. Effects of Passive Leg Raising on Pulse Pressure or on Stroke Volume are used to assess fluid responsiveness in patients suffering from shock states.
Sponsors & Collaborators
-
Centre Hospitalier Régional d'Orléans
lead OTHER
Principal Investigators
-
Thierry Boulain, MD · Centre Hospitalier Régional d'Orléans, France
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-01-16
- Primary Completion
- 2024-05-04
- Completion
- 2024-05-04
Countries
- France
Study Locations
More Related Trials
-
Changes in PPV Induced by PLR Test to Predict Fluid Responsiveness in ICU
NCT03225378 ·Status: COMPLETED
-
Use of a Mini-fluid Bolus to Identify Fluid Responsiveness
NCT03058653 ·Status: WITHDRAWN ·Phase: NA
-
Fluid Responsiveness Prediction at the Bedside
NCT00721604 ·Status: COMPLETED
-
VOLume and Vasopressor Therapy in Patients With Hemodynamic instAbility
NCT04089098 ·Status: COMPLETED
-
Timing and Dose of Fluid Deresuscitation in Critically Ill Patients
NCT07275658 ·Status: RECRUITING
-
Low Dose Vasopressin in Traumatic Shock
NCT00420407 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
Hypertonic Resuscitation Following Traumatic Injury
NCT00316017 ·Status: TERMINATED ·Phase: PHASE3
-
Ultrasound and Clinical Approach for the Dynamic Assessment of Fluid Tolerance in the Intensive Care Unit
NCT06415916 ·Status: RECRUITING
-
Diagnostic Accuracy of the Central Venous Pressure (CVP) Variation to Predict Fluid Responsiveness in Spontaneously Breathing Patients
NCT03780660 ·Status: COMPLETED
-
Validation of the Fluid Responsiveness Index in Critically Ill Patients
NCT00894309 ·Status: UNKNOWN
-
Effect of Fluid Deresuscitation With Central Venous Pressure Target 0-4 mmHg in Septic Shock Patients
NCT04156451 ·Status: COMPLETED ·Phase: NA
-
End-expiratory Occlusion Test and Lung Recruitment Maneuver to Assess Fluid responsiVeness In Surgical Patients
NCT03820440 ·Status: UNKNOWN ·Phase: NA
-
Preventing Cardiovascular collaPse With Administration of Fluid Resuscitation Before Endotracheal Intubation
NCT03026777 ·Status: COMPLETED ·Phase: PHASE4
-
The Impact of the Fluid Resuscitation on the Venous Volume and Flow Characteristics in Hypovolemic Shock
NCT02474056 ·Status: WITHDRAWN
-
PPV to Guide Fluid Management in the PICU
NCT02308371 ·Status: COMPLETED ·Phase: NA
-
Time Course Evolution of Cardiac Output
NCT03694717 ·Status: COMPLETED
-
Passive Leg Raise and Mini-fluid Challenge Effect on Various Cardiac Output Surrogates for Fluid Responsiveness
NCT06390423 ·Status: RECRUITING
-
Emergency Department (ED) Flow-directed Fluid Optimization Resuscitation Trial (EFFORT)
NCT01128413 ·Status: TERMINATED ·Phase: NA
-
Novel Device for Rapid Fluid Administration
NCT03074682 ·Status: COMPLETED ·Phase: NA
-
A Prospective Observational Study of the Expectations and Physiological Effects of Fluid Bolus Therapy
NCT03178578 ·Status: UNKNOWN
-
Optimization of Fluid Therapy in Sepsis by a Passive Leg Raising Test
NCT02301585 ·Status: TERMINATED ·Phase: NA
-
Hemodynamic Optimization By Non-Invasive Determination Of Cardiac Output In Critically Ill Patients
NCT01309724 ·Status: COMPLETED ·Phase: NA
-
Vasoactive Drugs in Intensive Care Unit
NCT02118467 ·Status: RECRUITING ·Phase: PHASE4
-
Comparison of the Effects of an Hypertonic Solution With Ringer Lactate on Right Ventricular Function Following Cardiac Surgery
NCT02782520 ·Status: COMPLETED ·Phase: PHASE3
-
Portal Vein Pulsatility Index to Assess Fluid Intolerance
NCT06440772 ·Status: COMPLETED