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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

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Study Design


Related Conditions & MeSH terms


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

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