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An Investigation of N-acetylcysteine and Fenoldopam as Renal Protection Agents for Cardiac Surgery

N-acetylcysteine and Fenoldopam Protect the Renal Function of Patients With Chronic Renal Insufficiency Undergoing Cardiac Surgery.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00122018
Enrollment
80
Registered
2005-07-21
Start date
2002-05-31
Completion date
2006-03-31
Last updated
2014-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgical Procedures, Kidney Failure, Acute, Kidney Failure, Chronic

Keywords

Kidney failure, Cardiac Surgery, Fenoldopam, N-acetylcysteine

Brief summary

Patients with abnormal kidney function are at increased risk for complications following heart surgery, including worsening kidney function possibly requiring dialysis, a prolonged stay in the critical care unit and hospital, and the increased risk of death. Prior attempts at kidney protection for heart surgery patients have had mixed results. Two medicines, fenoldopam and N-acetylcysteine, have been shown to protect kidney function in other circumstances that cause kidney stress. The purpose of this study is to determine whether these medications will help to maintain the function of diseased kidneys during heart surgery.

Detailed description

This is a randomized, double-blinded, placebo-controlled trial to evaluate fenoldopam and N-acetylcysteine (NAC) individually, and together, as renal protective agents for patients with renal insufficiency undergoing heart surgery. Subjects have chronic renal insufficiency with creatinine clearance (CrCl) \</= 40cc/min but not on pre-operative dialysis, and receive: NAC 600 mg by mouth (po) twice a day (bid) or placebo starting 24 hours pre-operative and continuing through the day of surgery; and/or fenoldopam 0.1 mcg/kg/min intravenous (IV) or saline placebo at anesthetic induction and continuing for 48 hours. Outcome data include: nadir, post-operative day 3 and post-operative day 14 CrCl, time to CrCl nadir, length of Intensive Care Unit (ICU) stay, length of post-operative hospital stay, hospital costs, mortality, and the need for hemodialysis. Intraoperative and post-operative pressor use is being monitored. The enrollment will include 80 patients (20 in each group).

Interventions

DRUGN-acetylcysteine

Sponsors

Abbott
CollaboratorINDUSTRY
Linda F. Barr, M.D.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Chronic creatinine clearance \</= 40cc/h * Pre-operative cardiac surgery

Exclusion criteria

* Pre-operative ongoing dialysis * Nausea and vomiting * Uncontrolled glaucoma * Allergy to metabisulfite * Enrollment in another clinical study within 30 days * Pregnancy * Acute renal failure

Design outcomes

Primary

MeasureTime frame
Length of post-operative hospital stay30-day
Length of post-operative critical care stay30-day
Creatinine clearance post-operative days 3, 14, and nadir14 day

Secondary

MeasureTime frame
Days to post-operative creatinine clearance nadir14 day
Mortality30-day
Intraoperative and post-operative pressor use (pressor-hours)48 hour
Hospital costs30-day

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026