search
Back to results

Acute Kidney Injury After Cardiac Surgery (NEPHROCAR)

Primary Purpose

Acute Kidney Injury, Cardiac Surgery

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Standard clinical routine
Nephrocheck test
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Acute Kidney Injury focused on measuring Urinary biomarkers, Intensive Care Unit

Eligibility Criteria

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

Inclusion Criteria:

  • On-pump cardiac surgery ;
  • Informed and written consent of the patient or inclusion according to the emergency procedure;
  • Affiliated patient or beneficiary of a social protection

Exclusion criteria:

  • Left and / or right ventricular assist device;
  • Heart transplant;
  • Chronic kidney disease with renal replacement therapy before surgery;
  • Hemorrhagic shock requiring surgical hemostasis at the time of randomization

Sites / Locations

  • Rennes University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control group

Nephrocheck group

Arm Description

Standard clinical routine

Nephrocheck test

Outcomes

Primary Outcome Measures

Occurence of an AKI according to the KDIGO classification without oliguria
According to the KDIGO classification: Stage 1; Increase in serum creatinine ≥ 26.5 μmol / l or 1.5 to 1.9 times baseline serum creatinine Stage 2; Increase in baseline serum creatinine from 2.0 to 2.9 times Stage 3; An increase of 3.0 times the baseline serum creatinine or serum creatinine ≥ 354 μmol / l or initiation of renal replacement therapy

Secondary Outcome Measures

Filling solute volumes
Recording of the filling solute volumes administered within 48 hours postoperatively
Use of catecholamin
Recording (YES/NO) of the recourse of catecholamin required during the medical care, within 48 hours postoperatively
Special extra corporeal circulation
Recording (YES/NO) of the recourse of a particular extracorporeal system within 48 hours postoperatively : Extracorporeal Life Support, heart pumps (Impela® like devices), or Intra-aortic balloon pump.
Duration of stay in the ward
Oliguria
Proportion of patients with an oliguria defined according to the KDIGO criteria : Stade 1 ; diuresis < 0.5 mL/kg/h for 6 à 12 h Stade 2 ; diuresis < 0.5 mL/kg/h for more than 12h Stade 3 ; diuresis < 0.3 mL/kg/h for more than 24h or anuria ≥ 12h ;
Repeatability of the Nephrocheck® test
Only for the patients in the Nephrocheck arm, variations between pre and postoperative Nephrocheck® test results will be assessed
Mortality rate
Mortality rate in the ward

Full Information

First Posted
December 15, 2017
Last Updated
December 1, 2021
Sponsor
Rennes University Hospital
Collaborators
JRAR Association
search

1. Study Identification

Unique Protocol Identification Number
NCT03396770
Brief Title
Acute Kidney Injury After Cardiac Surgery
Acronym
NEPHROCAR
Official Title
Impact of the Early Hemodynamic Evaluation Guided by Urinary Biomarkers on the Acute Kidney Injury After Cardiac Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
January 14, 2018 (Actual)
Primary Completion Date
September 16, 2021 (Actual)
Study Completion Date
September 16, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital
Collaborators
JRAR Association

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
Acute kidney injury (AKI) is common after cardiac surgery. The diagnosis is based on the criteria defined by the Kidney Disease Improving Global Outcomes (KDIGO) classification: oliguria and elevation of serum creatinine. However, oliguria is not specific of AKI and elevation of serum creatinine is too late. Therefore, new methods have been developed to earlier assess the risk of AKI. Among those methods, it has been shown that the increase of urinary dosage, in the hours following the surgery, of two proteins (Tissue Inhibitor of Metallo-Protease 2 (TIMP2) and Insulin Growth Factor Binding Protein 7 (IGFBP7)) is associated with an increased risk of occurrence of AKI in patients hospitalized in intensive care unit. The Nephrocheck® test combines the urinary dosage of those two proteins TIMP2 and IGFBP7. Insofar as post-surgery low cardiac output is one curable cause of AKI, the early detection of early kidney risk allows corrective measures to stabilize hemodynamic state and thus to reduce the risk of AKI.
Detailed Description
The usual diagnostic markers of AKI are defaulted. Indeed, oliguria tends to overstate the impact of AKI, up to 40-50% of patients. Postoperative increased serum creatinine is a late marker for the AKI. Furthermore, perioperative hemodilution and serum creatinine kinetic delay the postoperative peak of serum creatinine from 48 to 72 h. Nephrocheck® test combines the urinary dosage of 2 proteins (TIMP2 and IGFBP7). These 2 proteins are excreted by the tubular cell in case of suffering whatever the origin, for example tissue hypoxia by low renal blood flow or a systemic inflammatory response. In a medical ICU, the test performed within 4 to 12 hours after kidney aggression can predict the onset of persistent AKI beyond 4 weeks. Until randomization, all patients are treated according to the standard of care for the center. This includes a blood test upon arrival in the intensive care unit and continuous monitoring of vital parameters.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury, Cardiac Surgery
Keywords
Urinary biomarkers, Intensive Care Unit

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
open labeled randomized clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
848 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Standard clinical routine
Arm Title
Nephrocheck group
Arm Type
Experimental
Arm Description
Nephrocheck test
Intervention Type
Procedure
Intervention Name(s)
Standard clinical routine
Intervention Description
Patient management is carried out according to the usual service protocol
Intervention Type
Procedure
Intervention Name(s)
Nephrocheck test
Intervention Description
Nephrocheck® test is realized 4 hours after the end of the cardiopulmonary bypass If the test is positive, hemodynamic evaluation is carried out and adapted therapy to result of this evaluation is initiated. If the test is negative, patient management is carried out according to the usual protocol. A second test is realized 6 hours after the first test whatever the result of it.
Primary Outcome Measure Information:
Title
Occurence of an AKI according to the KDIGO classification without oliguria
Description
According to the KDIGO classification: Stage 1; Increase in serum creatinine ≥ 26.5 μmol / l or 1.5 to 1.9 times baseline serum creatinine Stage 2; Increase in baseline serum creatinine from 2.0 to 2.9 times Stage 3; An increase of 3.0 times the baseline serum creatinine or serum creatinine ≥ 354 μmol / l or initiation of renal replacement therapy
Time Frame
72 hours after surgery
Secondary Outcome Measure Information:
Title
Filling solute volumes
Description
Recording of the filling solute volumes administered within 48 hours postoperatively
Time Frame
48 hours after surgery
Title
Use of catecholamin
Description
Recording (YES/NO) of the recourse of catecholamin required during the medical care, within 48 hours postoperatively
Time Frame
48 hours after surgery
Title
Special extra corporeal circulation
Description
Recording (YES/NO) of the recourse of a particular extracorporeal system within 48 hours postoperatively : Extracorporeal Life Support, heart pumps (Impela® like devices), or Intra-aortic balloon pump.
Time Frame
48 hours after surgery
Title
Duration of stay in the ward
Time Frame
Up to 28 days post surgery
Title
Oliguria
Description
Proportion of patients with an oliguria defined according to the KDIGO criteria : Stade 1 ; diuresis < 0.5 mL/kg/h for 6 à 12 h Stade 2 ; diuresis < 0.5 mL/kg/h for more than 12h Stade 3 ; diuresis < 0.3 mL/kg/h for more than 24h or anuria ≥ 12h ;
Time Frame
48 hours after surgery
Title
Repeatability of the Nephrocheck® test
Description
Only for the patients in the Nephrocheck arm, variations between pre and postoperative Nephrocheck® test results will be assessed
Time Frame
10 hours post surgery
Title
Mortality rate
Description
Mortality rate in the ward
Time Frame
Up to 28 days post surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: On-pump cardiac surgery ; Informed and written consent of the patient or inclusion according to the emergency procedure; Affiliated patient or beneficiary of a social protection Exclusion criteria: Left and / or right ventricular assist device; Heart transplant; Chronic kidney disease with renal replacement therapy before surgery; Hemorrhagic shock requiring surgical hemostasis at the time of randomization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sébastien BIEDERMANN, MD
Organizational Affiliation
CHU Rennes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rennes University Hospital
City
Rennes
ZIP/Postal Code
35000
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Acute Kidney Injury After Cardiac Surgery

We'll reach out to this number within 24 hrs