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A Study of Two Iodinated Contrast Agents in Renally Impaired Patients Undergoing Cardiac Angiography

CIN Clinical Trial

Official title:
Visipaque and Isovue in Cardiac Angiography in Renally Impaired Patients

Clinical Trial Summary

The main purpose of this study is to compare the incidence of contrast induced nephrotoxicity following the administration of Isovue or Visipaque in patients with moderate to severe renal insufficiency undergoing cardiac angiography. Serum creatinine will be measured before and up to 48-72 hours after the administration of the contrast agent to evaluate renal function.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00289029
Study type Interventional
Source Bracco Diagnostics, Inc
Contact
Status Completed
Phase Phase 4
Start date July 2005
Completion date June 2006
View Details
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