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NCT Number: NCT00188630

N-Acetylcysteine for Preventing Renal Injury After Cardiac Surgery

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Toronto General Hospital, UHN

Toronto, Ontario, M5G 2C4, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

N-acetylcysteine

Drug

5% dextrose solution

Other

Primary outcomes

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

    Time frame: 72 hours following surgery

Secondary outcomes

  1. Maximum increase in serum creatinine concentration over first 72 hours following surgery.

    Time frame: 72 hours following surgery

  2. Increase in serum creatinine >= 0.5 mg/dL from baseline over first 72 hours following surgery (dichotomous outcome).

    Time frame: 72 hours following surgery

  3. 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

  4. Percent change in calculated creatinine clearance (Cockcroft-Gault formula) at hospital discharge.

    Time frame: hospital discharge

  5. Maximum percent decline in calculated creatinine clearance (Cockcroft-Gault formula) at 8 weeks following surgery.

    Time frame: 8 weeks followiing surgery

  6. 30-day need for renal replacement therapy

    Time frame: 30 day inclusive

  7. 30-day all-cause mortality

    Time frame: 30 day follow up

  8. Length of stay in intensive care unit (postoperative)

    Time frame: Duration of stay in the ICU

  9. Length of stay in hospital (postoperative)

    Time frame: Until discharge form hospital

  10. 24-hour fluid perioperative fluid balance

    Time frame: 24 hours

  11. 24-hour urine output

    Time frame: 24 hour

  12. Adverse perioperative event

    Time frame: Intra operative measure

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Collaborators

  • Heart and Stroke Foundation of Ontario

Registry information

Official study 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.

Important dates

Study start
2003
Primary completion
2007
Study completion
2007
First posted
Sep 16, 2005
Registry last updated
Apr 20, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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