drugset / Trial / NCT00908310

Post-marketing Safety Study in Patients With Moderate Renal Insufficiency Who Receive Omniscan for Contrast-enhanced Magnetic Resonance Imaging (MRI)

NCT00908310

Phase 4 Completed 213 enrolled GE Healthcare i3 Statprobe · collab
NaSingle-groupOpen-label

Summary

This will be an international, multi-center, post-marketing surveillance study in patients with moderate renal insufficiency who are administered gadodiamide, Omniscan, during a MRI. Omniscan will be administered intravenously at the medical discretion of the prescribing physician.

Timeline

Start
2009-05
Primary completion
2013-06
Completion
2013-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Gadodiamide Diagnostic / imaging agent Intravenous