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Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure (EarlyDry)

Primary Purpose

Acute Kidney Injury, Fluid Overload

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Fluid balance negativation
Body weight Stabilization
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Acute Kidney Injury focused on measuring Renal Replacement Therapy (RRT), Ultrafiltration, Deresuscitation, Fluid balance, Fluid overload, Tissue perfusion

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Acute kidney injury treated by continuous renal replacement therapy in ICU less than 7 days, At least 1 organ failure during ICU in addition to AKI (mechanical ventilation or vasopressors administration>12 hours), Cumulative UF net less than 1000ml before inclusion, Norepinephrine < 0,5 µg/kg/min, Absence of hypoperfusion signs, Fluid overload defined as follows : fluid overload > 5% of base weight (based on cumulative fluid balance or a weight gain) and/or peripheral edema (AKIKI edema scale > 2). Exclusion Criteria: Chronic renal failure hemodialyzed before admission to the ICU, Mechanical circulatory support (ECMO, LVAD), Pregnant, child -bearing age or lactating women, Stroke less than 30 days, Intestinal ischemia less than 7 days documented non-operated, Interventional study participation or exclusion period on going, Guardianship, curatorship or safeguard of justice, Absence of signature of free and informed consent by the patient and/or relative, Patients not affiliated to a social security scheme or beneficiaries of a similar scheme

Sites / Locations

  • Service d'Anesthesie-Réanimation, Hôpital Louis Pradel, Hospices Civils de Lyon
  • Service de Réanimation, CHU de Dijon
  • Service de Réanimation, Hôpital Michallon
  • Service Anesthésie Réanimation, Hôpital Edouard Herriot, Hospices Civils de Lyon
  • Service de Réanimation, Clinique de la Sauvegarde
  • Département d'anesthésie réanimation Hôpital Européen Georges Pompidou
  • Service de Réanimation, Centre Hospitalier Universitaire de Saint-Étienne

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Corrective strategy

Stabilizing strategy

Arm Description

In the experimental group, all patients will have a UFnet settled (2 ml/kg/h ) in order to reach the patient baseline body weight.

In the control group, all patients will have a UFnet 2 ml settled (0 to 1 ml/kg/h) in order to stabilize the patient body weight.

Outcomes

Primary Outcome Measures

Number of organ replacement free-days
Number of organ replacement free-days, i.e, number of renal replacement therapy-free days, number of vasopressor-free days, number of ventilator-free day. Number of days between 2 same type organ replacement interruption is not counted. In case of death before 30 days, number of days is censored to 0.

Secondary Outcome Measures

Mortality decrease
Number of deaths
Number of renal replacement therapy-free days increase
Number of renal replacement therapy-free days
Number of ventilator-free day increase
Number of ventilator-free day
Number of vasopressor-free day increase
Number of vasopressor-free day
Duration of intensive care unit stay
Number of days in ICU
SOFA score evolution
SOFA score : Sepsis-related Organ Failure Assessment, min : 0 max : 24 (worse)
Incidence of arrhythmias and cardiac conduction disorders in both group
Number of arrhythmias and cardiac conduction disorders occurrence on ECG
Incidence of intestinal ischemia in both group
Number of intestinal ischemia on CT scan or endoscopy
Incidence of strokes
Number of ischemic strokes occurrence on imagery
Incidence of delirium
Presence of delirium assessed with the CAM ICU scale : positive or negative score. A positive score means presence of delirium
Renal recovery assessment
Renal recovery is defined according to MAKE 30 scale : Survival Absence of renal replacement therapy Day 30 creatinine level < baseline creatinine x 200 %

Full Information

First Posted
April 5, 2023
Last Updated
April 26, 2023
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT05817539
Brief Title
Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure
Acronym
EarlyDry
Official Title
Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure in Intensive Care Unit. A Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
July 2025 (Anticipated)
Study Completion Date
July 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In Intensive Care Unit (ICU) patients with acute kidney injury (AKI) and treated with renal replacement therapy (RRT) often present a fluid overload which is associated with morbidity (mechanical ventilation duration increase, kidney recovery decrease) and mortality. Patients' prognostic could be improved by correcting the fluid overload with net ultrafiltration (UFnet) however it may lead to harmful iatrogenic hypovolemia responsible of deleterious ischemic lesions. In usual practice, UF net prescription are variable and there are different international recommendations. Some observational studies suggest that using a UFnet between 1 et 1.75 mL/kg/h in fluid overloaded patient decrease mortality. Fluid overload increases morbidity and mortality, particularly in RRT. Studies without RRT argue for an efficacy of management by decreasing the fluid overload .Cohort studies suggest to use a moderate UFnet instead of a low UFnet. Some data from studies on early versus late RRT that relate the fluid balance or correct the fluid overload during the early strategy argue for a beneficial effect of an early deresuscitation strategy Consequently, the impact of a moderate UFnet (to decrease the fluid overload) compared to a low UFnet (to stabilize the fluid overload) in a randomized interventional study could be assessed. The study hypothesis is that : an early fluid overload deresuscitation protocol with a high UFnet (2 ml/kg/h) targeting both the negativation of cumulated fluid balance to reach a dry weight and the maintenance of tissue perfusion. Compared to fluid overload deresuscitation protocol with a low UFnet (between 0 and 1 ml/kg/h) to reach a stabilization of cumulated fluid balance without monitoring the tissue perfusion. could improve overall, renal, hemodynamic and respiratory prognosis in fluid overloaded patients with renal replacement therapy in ICU

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury, Fluid Overload
Keywords
Renal Replacement Therapy (RRT), Ultrafiltration, Deresuscitation, Fluid balance, Fluid overload, Tissue perfusion

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
For this protocol, the double blind is impossible to set up. Clinicians in charge of patients and implementing the depletion strategy cannot be blinded. The patients will be blinded, they will not be aware of strategy applied. The medical staff will ensure that no information about the intervention is given to the patient.
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Corrective strategy
Arm Type
Experimental
Arm Description
In the experimental group, all patients will have a UFnet settled (2 ml/kg/h ) in order to reach the patient baseline body weight.
Arm Title
Stabilizing strategy
Arm Type
Other
Arm Description
In the control group, all patients will have a UFnet 2 ml settled (0 to 1 ml/kg/h) in order to stabilize the patient body weight.
Intervention Type
Procedure
Intervention Name(s)
Fluid balance negativation
Intervention Description
During the RRT, UFnet will be settled on 2ml/kg/h and adapted to hemodynamic tolerance and tissue perfusion . When the patient's baseline body weight is reached the UF net will be settled to maintain it. In case of failure of the fluid balance negativation after 24h, UFnet will be settled on 3ml/kg/h. Then when the baseline body weight is reached UFnet will be settled on 0.5 et 1ml/kg/h or if necessary adapted to 1,5ml/kg/h to maintain it In case of hemodynamic intolerance (NADN > 0,5 µg/kg/min) or tissue hypoperfusion, UF net will be stopped during 6 hours and restarted if NADN < 0,5 µg/kg/min and without tissue hypoperfusion.
Intervention Type
Procedure
Intervention Name(s)
Body weight Stabilization
Intervention Description
During the RRT, UFnet will be settled between 0 et 1 ml/kg/h and adapted in case of weight stabilization failure or hemodynamic intolerance. In case of weight stabilisation failure ( variation >5%), the UF net can be increased to 1,5 ml/kg/h. In case of hemodynamic intolerance (NADN > 0,5 µg/kg/min), UF net will be stopped during 6 hours and restarted if NADN < 0,5 µg/kg/min.
Primary Outcome Measure Information:
Title
Number of organ replacement free-days
Description
Number of organ replacement free-days, i.e, number of renal replacement therapy-free days, number of vasopressor-free days, number of ventilator-free day. Number of days between 2 same type organ replacement interruption is not counted. In case of death before 30 days, number of days is censored to 0.
Time Frame
Day 30
Secondary Outcome Measure Information:
Title
Mortality decrease
Description
Number of deaths
Time Frame
30 days
Title
Number of renal replacement therapy-free days increase
Description
Number of renal replacement therapy-free days
Time Frame
Day 30
Title
Number of ventilator-free day increase
Description
Number of ventilator-free day
Time Frame
Day 30
Title
Number of vasopressor-free day increase
Description
Number of vasopressor-free day
Time Frame
Day 30
Title
Duration of intensive care unit stay
Description
Number of days in ICU
Time Frame
Up to Day 30
Title
SOFA score evolution
Description
SOFA score : Sepsis-related Organ Failure Assessment, min : 0 max : 24 (worse)
Time Frame
From Day 0 up to Day 5
Title
Incidence of arrhythmias and cardiac conduction disorders in both group
Description
Number of arrhythmias and cardiac conduction disorders occurrence on ECG
Time Frame
From Day 0 up to Day 5
Title
Incidence of intestinal ischemia in both group
Description
Number of intestinal ischemia on CT scan or endoscopy
Time Frame
From Day 0 to Day 30
Title
Incidence of strokes
Description
Number of ischemic strokes occurrence on imagery
Time Frame
From Day 0 to Day 30
Title
Incidence of delirium
Description
Presence of delirium assessed with the CAM ICU scale : positive or negative score. A positive score means presence of delirium
Time Frame
Between Day 0 and Day 5
Title
Renal recovery assessment
Description
Renal recovery is defined according to MAKE 30 scale : Survival Absence of renal replacement therapy Day 30 creatinine level < baseline creatinine x 200 %
Time Frame
Day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute kidney injury treated by continuous renal replacement therapy in ICU less than 7 days, At least 1 organ failure during ICU in addition to AKI (mechanical ventilation or vasopressors administration>12 hours), Cumulative UF net less than 1000ml before inclusion, Norepinephrine < 0,5 µg/kg/min, Absence of hypoperfusion signs, Fluid overload defined as follows : fluid overload > 5% of base weight (based on cumulative fluid balance or a weight gain) and/or peripheral edema (AKIKI edema scale > 2). Exclusion Criteria: Chronic renal failure hemodialyzed before admission to the ICU, Mechanical circulatory support (ECMO, LVAD), Pregnant, child -bearing age or lactating women, Stroke less than 30 days, Intestinal ischemia less than 7 days documented non-operated, Interventional study participation or exclusion period on going, Guardianship, curatorship or safeguard of justice, Absence of signature of free and informed consent by the patient and/or relative, Patients not affiliated to a social security scheme or beneficiaries of a similar scheme
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias JACQUET LAGREZE, MD PhD
Phone
04 72 35 79 41
Ext
+33
Email
Matthias.jacquet-lagreze@chu-lyon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Julia CANTERINI, project manager
Phone
04 27 85 66 28
Ext
+33
Email
Julia.canterini@chu-lyon.fr
Facility Information:
Facility Name
Service d'Anesthesie-Réanimation, Hôpital Louis Pradel, Hospices Civils de Lyon
City
Bron
ZIP/Postal Code
69500
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthias JACQUET LAGREZE, MD
Phone
04 72 35 79 41
Ext
+33
Email
Matthias.jacquet-lagreze@chu-lyon.fr
Facility Name
Service de Réanimation, CHU de Dijon
City
Dijon
ZIP/Postal Code
21000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre-Grégoire GUINOT, MD
Phone
03 80 29 56 03
Ext
+33
Email
pierregregoire.guinot@chu-dijon.fr
Facility Name
Service de Réanimation, Hôpital Michallon
City
La Tronche
ZIP/Postal Code
38700
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Géraldine DESSERTAINE, MD
Phone
04 76 76 75 88
Ext
+33
Email
GDessertaine@chu-grenoble.fr
Facility Name
Service Anesthésie Réanimation, Hôpital Edouard Herriot, Hospices Civils de Lyon
City
Lyon
ZIP/Postal Code
69003
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas RIMMELE, MD-PHD
Phone
04 72 11 11 96
Ext
+33
Email
thomas.rimmele@chu-lyon.fr
Facility Name
Service de Réanimation, Clinique de la Sauvegarde
City
Lyon
ZIP/Postal Code
69009
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Olivier DESEBBE, MD
Phone
04 78 64 06 50
Ext
+33
Email
oldesebbe@yahoo.com
Facility Name
Département d'anesthésie réanimation Hôpital Européen Georges Pompidou
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicolas POLGE, MD
Phone
01 56 09 34 25
Ext
+33
Email
nicolas.polge@aphp.fr
Facility Name
Service de Réanimation, Centre Hospitalier Universitaire de Saint-Étienne
City
Saint-Étienne
ZIP/Postal Code
42055
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jérôme MOREL, MD-PHD
Phone
04 77 12 03 88
Ext
+33
Email
jerome.morel@chu-st-etienne.fr

12. IPD Sharing Statement

Plan to Share IPD
No

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Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure

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