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A Study to Explore the Renal Safety of Visipaque Injection 320 mgI/mL in Patients With Chronic Kidney Disease

Chronic Kidney Diseases Clinical Trial

Official title:
Parallel-Group, Placebo-Controlled Randomized Study Investigating the Effect of Intravenous Iso-osmolar Iodinated Contrast Material Iodixanol (Visipaque™ Injection 320 mgI/mL) on Renal Function in Adults With Chronic Kidney Disease (CKD) Stage III or Stage IV Who Have Undergone Endovascular Aneurysm Repair (EVAR)

Clinical Trial Summary

This parallel-group, randomized, placebo-controlled study will examine the incidence and severity of acute kidney injury (AKI) in patients with chronic kidney disease (CKD) stage III/IV following an i.v. injection of iso-osmolar iodinated contrast material iodixanol (Visipaque™ Injection 320 mgI/mL), as compared with patients who received saline and underwent a non-enhanced CT (NECT) and duplex ultrasound (US) during their scheduled post-EVAR surveillance imaging.

Clinical Trial Description

GEHC has decided not to provide this detail ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03119662
Study type Interventional
Source GE Healthcare
Contact
Status Terminated
Phase Phase 4
Start date February 8, 2018
Completion date October 19, 2018
View Details
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