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Early RRT in AKI After Cardiac Surgery

Primary Purpose

Acute Kidney Injury

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Renal replacement therapy
Best medical management
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Kidney Injury focused on measuring Acute Kidney Injury, Post Cardiac Surgery, Renal Replacement Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Patients within 7 days after cardiac surgery
  • Acute kidney injury (AKI) described as Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 (urine output <0.5mL/kg/h for ≥6h or 2-fold increase in serum creatinine compared with baseline)

Exclusion Criteria:

  • previous renal replacement therapy
  • AKI secondary to obstructive nephropathy
  • previous kidney transplantation

Sites / Locations

  • Seoul National University Bundang HospitalRecruiting
  • Seoul National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Early RRT group

Delayed RRT group

Arm Description

Patients who will undergo renal replacement therapy (RRT) within 6 hours of diagnosis of stage 2 acute kidney injury (AKI).

Patients who will undergo renal replacement therapy (RRT) if one of the absolute indications for RRT is present.

Outcomes

Primary Outcome Measures

Number of participants with operative mortality
any death, regardless of cause, occurring (1) within 30 days after surgery in or out of the hospital, and (2) after 30 days during the same hospitalization subsequent to the operation

Secondary Outcome Measures

Overall survival
overall survival
Number of participants with cardiovascular mortality
Any death related to cardiac events, including sudden death during follow-up
Number of participants with renal replacement therapy dependency
Number of participants who still needs renal replacement therapy at 90 days after operation.
Number of participants with major adverse kidney events (MAKE)
MAKE indicates the composite of death, need of renal replacement therapy, and persistent renal dysfunction.
Number of participants with renal replacement therapy related morbidity
adverse events related to renal replacement therapy (RRT) or vascular access for RRT.
Duration of mechanical ventilation
duration of mechanical ventilator support
Duration of intensive care unit stay
duration of intensive care unit stay
Hospital length of stay
hospital length of stay

Full Information

First Posted
December 10, 2021
Last Updated
April 10, 2023
Sponsor
Seoul National University Hospital
Collaborators
Seoul National University Bundang Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05175053
Brief Title
Early RRT in AKI After Cardiac Surgery
Official Title
Early Application of Renal-Replacement Therapy in Patients With Acute Kidney Injury After Cardiac Surgery: A Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 24, 2021 (Actual)
Primary Completion Date
September 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
Collaborators
Seoul National University Bundang Hospital

4. Oversight

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

5. Study Description

Brief Summary
Acute kidney injury (AKI) is one of the major complications after cardiac surgery that may affects 20% to 40% of patients according to the definitions. Also, AKI after cardiac surgery is associated with high morbidity and mortality, with eight-fold increase in the odds ratio of death when renal replacement therapy (RRT) is required. However the indication and the optimal timing of RRT initiation are still controversial. We hypothesized that a strategy of early initiation of RRT would result in a lower risk of surgical mortality than a standard strategy in post cardiac surgery patients with AKI of Kidney Disease: Improving Global Outcomes (KDIGO) classification stage 2 (serum creatinine, 2.0 times the baseline level; urine output, <0.5mL/kg/h for 6 or more hours).
Detailed Description
This trial was designed as a multi-center randomized, controlled trial to recruit 202 patients who develop acute kidney injury (AKI) described as Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 (serum creatinine, 2.0 times the baseline level; urine output, <0.5mL/kg/h for 6 or more hours) after cardiac surgery. Patients were randomized in a 1:1 ratio to 1 of the 2 treatment groups (Early vs. Delayed renal replacement therapy (RRT)) using a computerized system. Sample size determination : power calculation were performed based on the primary end point (operative mortality). The expected operative mortality in the control group with delayed initiation of RRT was 55% based on the literature. Differences between treatment groups were to be detected with a power of 80%, if the operative mortality of with early initiation of RRT was 35% or less. The expected treatment effect of 20% was calculated on the mortality differences between early and delayed RRT reported in previous studies. A required sample size for the final analysis was 101 patients per treatment group, 202 patients in total (level of significance, α = 0.05; type II error, β= 0.02; potential dropouts= 5%). Early RRT was initiated within 6 hours of diagnosis of stage 2 AKI. Delayed RRT was initiated if any one of the following absolute indications for RRT is present serum urea level higher than 100mg/dL and/or with uremic encephalopathy serum potassium level higher than 6mmol/L and/or with electrocardiography abnormalities urine production lower than 0.3mL/kg/hr for 24 hours pH of 7.15 or less and/or severe hypotension due to metabolic acidosis organ edema in the presence of AKI resistant to diuretic treatment. The primary end point is operative mortality (described as any death, regardless of cause, occurring (1) within 30 days after surgery in or out of the hospital, and (2) after 30 days during the same hospitalization subsequent to the operation). The secondary end points included 90 day overall survival, cardiovascular mortality, RRT dependence, and major adverse kidney events (MAKE), adverse events related to RRT or vascular access, duration of mechanical ventilator support and intensive care unit stay, and hospital length of stay. RRT delivery : Once RRT was initiated, both groups were treated using continuous venovenous hemodiafiltration (CVVHDF) with identical settings. Initial target dose of hemodiafiltration was 25 to 50mL/kg/hr depends on the decision of attending physician and further adjusted according to the metabolic needs of the patient. Replacement fluid was delivered into the extracorporeal circuit before the filter with a ratio of dialysate to replacement fluid of 1:1. Blood flow was maintained between 100 to 250mL/min. Regional anticoagulation with nafamostat (dosage 20-50mg/hr) was used to prevent circuit clotting if necessary. RRT was discontinued if renal recovery defined by urine output (>1mL/Kg/hr for 8 hours or more or >1000mL/24h without diuretics; >2000mL/24h with diuretics) and creatinine clearance (>20mL/min) occurred. If cessation criteria were not fulfilled after 7 days, conversion to intermittent hemodialysis would be considered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Acute Kidney Injury, Post Cardiac Surgery, Renal Replacement Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
202 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Early RRT group
Arm Type
Experimental
Arm Description
Patients who will undergo renal replacement therapy (RRT) within 6 hours of diagnosis of stage 2 acute kidney injury (AKI).
Arm Title
Delayed RRT group
Arm Type
Active Comparator
Arm Description
Patients who will undergo renal replacement therapy (RRT) if one of the absolute indications for RRT is present.
Intervention Type
Other
Intervention Name(s)
Renal replacement therapy
Intervention Description
Continuous renal replacement therapy using continuous venovenous hemodiafiltration (CVVHDF)
Intervention Type
Other
Intervention Name(s)
Best medical management
Intervention Description
The best medical management continues until the patient meets absolute indication of renal replacement therapy
Primary Outcome Measure Information:
Title
Number of participants with operative mortality
Description
any death, regardless of cause, occurring (1) within 30 days after surgery in or out of the hospital, and (2) after 30 days during the same hospitalization subsequent to the operation
Time Frame
at postoperative 30 days
Secondary Outcome Measure Information:
Title
Overall survival
Description
overall survival
Time Frame
at postoperative 90 days
Title
Number of participants with cardiovascular mortality
Description
Any death related to cardiac events, including sudden death during follow-up
Time Frame
at postoperative 90 days
Title
Number of participants with renal replacement therapy dependency
Description
Number of participants who still needs renal replacement therapy at 90 days after operation.
Time Frame
at postoperative 90 days
Title
Number of participants with major adverse kidney events (MAKE)
Description
MAKE indicates the composite of death, need of renal replacement therapy, and persistent renal dysfunction.
Time Frame
at postoperative 90 days
Title
Number of participants with renal replacement therapy related morbidity
Description
adverse events related to renal replacement therapy (RRT) or vascular access for RRT.
Time Frame
at postoperative 90 days
Title
Duration of mechanical ventilation
Description
duration of mechanical ventilator support
Time Frame
at postoperative 30 days
Title
Duration of intensive care unit stay
Description
duration of intensive care unit stay
Time Frame
at postoperative 30 days
Title
Hospital length of stay
Description
hospital length of stay
Time Frame
at postoperative 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients within 7 days after cardiac surgery Acute kidney injury (AKI) described as Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 (urine output <0.5mL/kg/h for ≥6h or 2-fold increase in serum creatinine compared with baseline) Exclusion Criteria: previous renal replacement therapy AKI secondary to obstructive nephropathy previous kidney transplantation
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ho Young Hwang, MD, PhD
Phone
82-2-2072-3020
Email
scalpel@hanmail.net
First Name & Middle Initial & Last Name or Official Title & Degree
Sue Hyun Kim, MD
Phone
82-2-2072-0358
Email
annesue01@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ho Young Hwang, MD, PhD
Organizational Affiliation
Seoul National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seoul National University Bundang Hospital
City
Seongnam
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dong Jung Kim, MD
Phone
82-31-787-7139
Email
mdknockout@gmail.com
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ho Young Hwang, MD, PhD
Phone
82-2-2072-3020
Email
scalpel@hanmail.net
First Name & Middle Initial & Last Name & Degree
Sue Hyun Kim, MD
Phone
82-2-2072-0358
Email
annesue01@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared because it is not allowed by our institutional IRB.

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Early RRT in AKI After Cardiac Surgery

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