Kidney Damage in Patients With Normal eGFR

Status Completed

Clinical Trial Summary

This is a pilot study, randomized, double-blind, parallel group comparison of two iodinated contrast agents used during percutaneous coronary intervention (PCI). All patients enrolled must have normal eGFR. Statistical summaries will be presented to analyse the various laboratory tests for the two groups.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01137786
Study type	Interventional
Source	Bracco Diagnostics, Inc
Contact
Status	Completed
Phase	Phase 4
Start date	December 2010
Completion date	April 2012

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