Clinical Trials Directory

Trials / Completed

CompletedNCT00211653

Acetylcysteine in the Prevention of Renal Failure After Bypass Surgery

Single Center Randomized Clinical Trial of the Effects of Acetylcysteine in the Prevention of Postoperative Renal Failure

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
102 (actual)
Sponsor
Minneapolis Veterans Affairs Medical Center · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if Acetylcysteine is effective in preventing renal failure associated with cardiac surgery

Detailed description

Postoperative renal dysfunction is a predictor of significant morbidity and mortality among patients undergoing cardiac surgery. The mortality associated with coronary artery by-pass surgery increases from 2% to almost 19% in patients with renal failure and approaches 60% in patients who require hemodialysis. Patients with preoperative renal dysfunction referred for coronary artery by pass surgery have an extraordinarily high risk of requiring postoperative dialysis. For example, among those patients with preoperative creatinine \>2.5 mg/dL, almost 50% require hemodialysis. Comparison: N-Acetylcysteine is superior to placebo in preventing renal failure after cardiac surgery

Conditions

Interventions

TypeNameDescription
DRUGN-Acetylcysteine

Timeline

Start date
2003-04-01
Completion
2006-11-01
First posted
2005-09-21
Last updated
2007-09-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00211653. Inclusion in this directory is not an endorsement.