N-Acetylcysteine for Preventing Renal Injury After Cardiac Surgery
Heart Disease, Acute Renal Failure
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
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
Active Comparator
Placebo Comparator
N-Acetylcysteine
Placebo
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.