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Contrast-induced Nephropathy clinical trials

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NCT ID: NCT00292487 Completed - Clinical trials for Contrast Induced Nephropathy

Patients With Renal Impairment Undergoing CT

Start date: November 2004
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare the incidence of contrast induced nephrotoxicity following the administration of Isovue or Visipaque in patients with mild to moderate renal impairment who undergo a clinically indicated IV contrast-enhanced (multidetector computed tomography) MDCT of the liver or MDCT angiography of the lower extremities. Serum Creatinine (SCr) will be measured before and up to 48-72 hours post dose.

NCT ID: NCT00237614 Completed - Clinical trials for Acute Myocardial Infarction

Contrast Nephropathy Prevention With N-Acetylcysteine in Acute Myocardial Infarction

Start date: February 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Patients with acute myocardial infarction undergoing primary angioplasty are at high risk for renal injury due to the toxic effect of contrast agents. Patients developing renal dysfunction after primary angioplasty have worse outcome. To investigate the role of the antioxidant N-acetylcysteine (NAC) in preventing renal injury in angioplasty, we randomized 352 consecutive patients undergoing primary angioplasty into three groups: the first group received NAC at standard dose (NAC group, 600 mg i.v. bolus before primary angioplasty, followed by oral 600 mg twice daily for the following 48 hours; n=115), the second group received NAC at double dose (DD-NAC group; 1,200 mg i.v. bolus and oral 1,200 mg twice daily for 48 hours; n=118), and the last group received placebo (controls; n=119).

NCT ID: NCT00175227 Completed - Clinical trials for Chronic Renal Failure

Prevention of Contrast-Induced Nephropathy

Start date: May 1996
Phase: N/A
Study type: Interventional

Patients with pre-existing kidney disease are at high risk of acute renal failure when exposed to radio-contrast dyes, for example during a cardiac angiogram. The investigators hypothesize that an infusion of saline + furosemide + mannitol will reduce rates of contrast-induced nephropathy when compared with saline infusion controls.