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N-Acetylcysteine for Preventing Renal Injury After Cardiac Surgery

Primary Purpose

Heart Disease, Acute Renal Failure

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
N-acetylcysteine
5% dextrose solution
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Heart Disease focused on measuring Cardiac Surgery, Acute Renal Failure, N-acetylcysteine, Cardiopulmonary bypass

Eligibility Criteria

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

Inclusion Criteria: CABG surgery under cardiopulmonary bypass AND/OR Valve replacement/repair surgery under cardiopulmonary bypass Preoperative creatinine clearance (Cockcroft-Gault equation) <= 60 mL/min. Age above 18 years Informed consent Exclusion Criteria: Preoperative need for renal replacement therapy Preoperative serum creatinine concentration >= 300 mmol/L Prior adverse reaction to NAC with significant systemic symptoms (generalized rash, urticaria, bronchospasm, hypotension) Preoperative intra-aortic balloon pump support and/or inotropes/vasopressors Recent coronary angiography or intravenous dye exposure (<= 24 hours) preceding surgery Planned intraoperative deep hypothermic circulatory arrest Pregnancy Chronic hepatitis or hepatic cirrhosis

Sites / Locations

  • Toronto General Hospital, UHN

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

N-Acetylcysteine

Placebo

Arm Description

IV NAC as a 100mg/kg bolus at the start of the surgical procedure (prior to the initiation of CPB), followed by a 10 mg/kg/hr infusion until 4 hours after completion of surgery

The control arm will instead receive placebo (5% dextrose solution), both as a bolus and infusion.

Outcomes

Primary Outcome Measures

Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) in first 72 hours following surgery.

Secondary Outcome Measures

Maximum increase in serum creatinine concentration over first 72 hours following surgery.
Increase in serum creatinine >= 0.5 mg/dL from baseline over first 72 hours following surgery (dichotomous outcome).
Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) >= 25% in first 72 hours following surgery (dichotomous outcome).
Percent change in calculated creatinine clearance (Cockcroft-Gault formula) at hospital discharge.
Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) at 8 weeks following surgery.
30-day need for renal replacement therapy
30-day all-cause mortality
Length of stay in intensive care unit (postoperative)
Length of stay in hospital (postoperative)
24-hour fluid perioperative fluid balance
24-hour urine output
Adverse perioperative event

Full Information

First Posted
September 9, 2005
Last Updated
April 19, 2011
Sponsor
University Health Network, Toronto
Collaborators
Heart and Stroke Foundation of Ontario
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1. Study Identification

Unique Protocol Identification Number
NCT00188630
Brief Title
N-Acetylcysteine for Preventing Renal Injury After Cardiac Surgery
Official Title
The PRIME (Perioperative Renal Insufficiency Management) Study: A Randomized, Double-blinded, Placebo-controlled Trial of N-acetylcysteine for Preventing Renal Injury After Cardiac Surgery.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Completed
Study Start Date
July 2003 (undefined)
Primary Completion Date
February 2007 (Actual)
Study Completion Date
July 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Health Network, Toronto
Collaborators
Heart and Stroke Foundation of Ontario

4. Oversight

5. Study Description

Brief Summary
Cardiac surgery improves the survival and quality of life of people with heart disease. Nonetheless, several complications continue to adversely affect outcomes following cardiac surgery. Kidney failure is a particularly important complication that is associated with increased death and duration of hospitalization. The most severe form of postoperative kidney failure, the need for dialysis, is uncommon at present. It is however likely to increase in the future. Patients undergoing cardiac surgery are getting older with more heart failure, diabetes, high blood pressure, and pre-existing kidney disease. Given that these are risk factors for postoperative kidney injury, dialysis rates will likely increase. Although multiple therapies have been tested, none have prevented postoperative kidney failure. N-acetylcysteine (NAC) is a drug that is commonly used to treat Tylenol overdoses. Over the past 2 years, it has also been used to prevent kidney damage after exposure to IV dye. There is good evidence that NAC will reduce kidney damage after IV dye exposure. There are strong reasons to believe that NAC may also prevent postoperative kidney failure. NAC is safe. Its major side-effects are allergic reactions, but serious reactions are rare. Since dialysis is uncommon, large studies are needed to determine if NAC prevents postoperative dialysis. In this situation, a pilot study is needed to determine if such a large trial is feasible. This proposal describes a pilot study. We will determine NAC's effects on creatinine clearance, a measure of how well the kidney works. Reduced creatinine clearance is closely related to dialysis and death after cardiac surgery. This biological marker allows us to determine NAC's effects on kidney function with a reduced sample size. If NAC improves creatinine clearance, it would suggest that NAC prevents postoperative dialysis, and would justify a larger study. A pilot study will help us estimate how many patients will be willing to participate in similar studies, vital for planning a future large study. Finally, our results will estimate how well NAC will reduce dialysis rates. This is needed for calculating the sample size for future studies.The study design is a randomized, double-blinded, placebo-controlled clinical trial among patients undergoing bypass surgery or heart valve surgery at the Toronto General Hospital (Toronto, ON). We will recruit 176 people who are at increased risk for developing kidney failure after surgery. Participants will receive either NAC or sugar solution during their operation. If participants have returned home within a month of surgery, they will be contacted at home on the 30th day after surgery to determine if they had any kidney-related problems since returning home. All participants will return to the Toronto General Hospital (TGH) during the 8th week after surgery for creatinine blood test and weight.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Disease, Acute Renal Failure
Keywords
Cardiac Surgery, Acute Renal Failure, N-acetylcysteine, Cardiopulmonary bypass

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
176 (Actual)

8. Arms, Groups, and Interventions

Arm Title
N-Acetylcysteine
Arm Type
Active Comparator
Arm Description
IV NAC as a 100mg/kg bolus at the start of the surgical procedure (prior to the initiation of CPB), followed by a 10 mg/kg/hr infusion until 4 hours after completion of surgery
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
The control arm will instead receive placebo (5% dextrose solution), both as a bolus and infusion.
Intervention Type
Drug
Intervention Name(s)
N-acetylcysteine
Intervention Type
Other
Intervention Name(s)
5% dextrose solution
Primary Outcome Measure Information:
Title
Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) in first 72 hours following surgery.
Time Frame
72 hours following surgery
Secondary Outcome Measure Information:
Title
Maximum increase in serum creatinine concentration over first 72 hours following surgery.
Time Frame
72 hours following surgery
Title
Increase in serum creatinine >= 0.5 mg/dL from baseline over first 72 hours following surgery (dichotomous outcome).
Time Frame
72 hours following surgery
Title
Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) >= 25% in first 72 hours following surgery (dichotomous outcome).
Time Frame
72 hours following surgery
Title
Percent change in calculated creatinine clearance (Cockcroft-Gault formula) at hospital discharge.
Time Frame
hospital discharge
Title
Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) at 8 weeks following surgery.
Time Frame
8 weeks followiing surgery
Title
30-day need for renal replacement therapy
Time Frame
30 day inclusive
Title
30-day all-cause mortality
Time Frame
30 day follow up
Title
Length of stay in intensive care unit (postoperative)
Time Frame
Duration of stay in the ICU
Title
Length of stay in hospital (postoperative)
Time Frame
Until discharge form hospital
Title
24-hour fluid perioperative fluid balance
Time Frame
24 hours
Title
24-hour urine output
Time Frame
24 hour
Title
Adverse perioperative event
Time Frame
Intra operative measure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CABG surgery under cardiopulmonary bypass AND/OR Valve replacement/repair surgery under cardiopulmonary bypass Preoperative creatinine clearance (Cockcroft-Gault equation) <= 60 mL/min. Age above 18 years Informed consent Exclusion Criteria: Preoperative need for renal replacement therapy Preoperative serum creatinine concentration >= 300 mmol/L Prior adverse reaction to NAC with significant systemic symptoms (generalized rash, urticaria, bronchospasm, hypotension) Preoperative intra-aortic balloon pump support and/or inotropes/vasopressors Recent coronary angiography or intravenous dye exposure (<= 24 hours) preceding surgery Planned intraoperative deep hypothermic circulatory arrest Pregnancy Chronic hepatitis or hepatic cirrhosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William S Beattie, MD
Organizational Affiliation
Toronto General Hospital, University Health Network
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toronto General Hospital, UHN
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
19384218
Citation
Wijeysundera DN, Karkouti K, Rao V, Granton JT, Chan CT, Raban R, Carroll J, Poonawala H, Beattie WS. N-acetylcysteine is associated with increased blood loss and blood product utilization during cardiac surgery. Crit Care Med. 2009 Jun;37(6):1929-34. doi: 10.1097/CCM.0b013e31819ffed4.
Results Reference
derived

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N-Acetylcysteine for Preventing Renal Injury After Cardiac Surgery

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