Biomarker Guided Intervention for Prevention of Acute Kidney Injury (BigpAK)
Primary Purpose
Acute Kidney Injury
Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Ionosteril
Sponsored by
About this trial
This is an interventional prevention trial for Acute Kidney Injury focused on measuring renal replacement therapy
Eligibility Criteria
"Inclusion Criteria":
- major surgery with a duration > 4 hours plus one of the following criteria:
- age > 75 years, or
- sepsis, or
- shock, or
- polytrauma, or
- need for invasive ventilation or catecholamines, or
- intra-operative application of contrast-medium, or
- preexisting chronic kidney disease (CKD1-4),
- informed consent
Exclusion Criteria:
- age < 18 years,
- end stage renal disease (ESRD),
- preexisting dialysis,
- withdrawal of consent,
- pregnancy,
- breastfeeding
Sites / Locations
- University Hospital Center Regensburg
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
standard care
interventional care
Arm Description
Patients in the standard care population receive - if biomarkers are elevated -treatment of AKI in accordance with KDIGO 2012 guidelines
Patients in the interventional population receive - if biomarkers are elevated - individualized treatment/volume substitution (balanced electrolyte solution = Ionosteril; 1,25-5 ml/kg/bw/6 hours) ) on the basis of predefined criteria
Outcomes
Primary Outcome Measures
Incidence and severity of AKI in both group
incidence and severity of AKI according to AKI network definition within 90 days will be monitored
Secondary Outcome Measures
need for renal replacement therapy,
Number of participants with a need for renal replacement therapy (defined as dialysis within 90 days)
length of ICU stay
overall length of ICU stay
length of hospital stay
overall length of ICU stay
ICU and hospital costs
to account for resulting costs, ICU and hospital cost of the standard care and the interventional patient population are monitored
incidence of chronic kidney disease (CKD)
Investigators want to see if there are any differences on resulting renal function - different stages of chronic kidney disease (CKD I-V) as a consequence of the performed therapy: standard care accoring to KDIGO guidelines versus interventional care
death
overall mortality
Full Information
NCT ID
NCT02500394
First Posted
July 7, 2015
Last Updated
May 4, 2017
Sponsor
University Hospital Regensburg
1. Study Identification
Unique Protocol Identification Number
NCT02500394
Brief Title
Biomarker Guided Intervention for Prevention of Acute Kidney Injury
Acronym
BigpAK
Official Title
Biomarker Guided Intervention to Prevent Development of Acute Kidney Injury in High-risk Surgical Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
June 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
January 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Regensburg
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the impact of a biomarked guided intervention on the development of acute kidney injury in high risk surgical patients. Eligible patients are screened for marker of tubular stress in the urine; if patient specific results are above a pre-defined cutoff they are randomized into a standard care group or an interventional group in which patients receive intensified volume therapy.
Detailed Description
This study evaluates the impact of a biomarked guided intervention on the development of acute kidney injury in high risk surgical patients.Used markers have been identified as markers of tubular stress and have been validated in previous studies with more than 1500 patients. The advantage of a biomarker guided approach is the saving of time for the diagnosis a developing acute kidney injury (AKI) in high risk surgical patients, since clinical signs of AKI (rise in creatinine/decline of estimated Glomerular Filtration Rate (eGFR), decline of diuresis). If used biomarkers are above a predefined cutoff within < 4 hours after surgery, patients are randomized in to a standard care population receiving treatment in accordance with Kidney Disease Improving Global Outcomes (KDIGO) guidelines. In the intervention population patients receive individual volume therapy (= balanced electrolyte solution (Ionosteril)) (1,25 ml/kg bw up to 5 ml/kg bw for 6 hours). Degree of volume therapy is estimated by several predifined parameters, e.g. central venous pressure (CVP).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
renal replacement therapy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
135 (Actual)
8. Arms, Groups, and Interventions
Arm Title
standard care
Arm Type
Placebo Comparator
Arm Description
Patients in the standard care population receive - if biomarkers are elevated -treatment of AKI in accordance with KDIGO 2012 guidelines
Arm Title
interventional care
Arm Type
Active Comparator
Arm Description
Patients in the interventional population receive - if biomarkers are elevated - individualized treatment/volume substitution (balanced electrolyte solution = Ionosteril; 1,25-5 ml/kg/bw/6 hours) ) on the basis of predefined criteria
Intervention Type
Procedure
Intervention Name(s)
Ionosteril
Intervention Description
biomarker guided volume substitution with Ionosteril
Primary Outcome Measure Information:
Title
Incidence and severity of AKI in both group
Description
incidence and severity of AKI according to AKI network definition within 90 days will be monitored
Time Frame
90 days
Secondary Outcome Measure Information:
Title
need for renal replacement therapy,
Description
Number of participants with a need for renal replacement therapy (defined as dialysis within 90 days)
Time Frame
90 days
Title
length of ICU stay
Description
overall length of ICU stay
Time Frame
90 days
Title
length of hospital stay
Description
overall length of ICU stay
Time Frame
90 days
Title
ICU and hospital costs
Description
to account for resulting costs, ICU and hospital cost of the standard care and the interventional patient population are monitored
Time Frame
90 days
Title
incidence of chronic kidney disease (CKD)
Description
Investigators want to see if there are any differences on resulting renal function - different stages of chronic kidney disease (CKD I-V) as a consequence of the performed therapy: standard care accoring to KDIGO guidelines versus interventional care
Time Frame
90 days
Title
death
Description
overall mortality
Time Frame
90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
"Inclusion Criteria":
major surgery with a duration > 4 hours plus one of the following criteria:
age > 75 years, or
sepsis, or
shock, or
polytrauma, or
need for invasive ventilation or catecholamines, or
intra-operative application of contrast-medium, or
preexisting chronic kidney disease (CKD1-4),
informed consent
Exclusion Criteria:
age < 18 years,
end stage renal disease (ESRD),
preexisting dialysis,
withdrawal of consent,
pregnancy,
breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tobias Bergler, MD
Organizational Affiliation
UKR-Department of Nephrology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ivan Göcze, MD
Organizational Affiliation
UKR-Department of Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Center Regensburg
City
Regensburg
ZIP/Postal Code
93042
Country
Germany
12. IPD Sharing Statement
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Biomarker Guided Intervention for Prevention of Acute Kidney Injury
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