This is a multi-center sample analysis study in which urine samples previously collected from apparently healthy adult subjects, and subjects with stable chronic morbidities but without AKI in order to establish the reference range for the VIDAS® NEPHROCLEAR™ CCL14 test.
The VIDAS® NEPHROCLEAR™ CCL14 Test is intended to be used in conjunction with clinical evaluation, in ICU patients with moderate to severe (stage 2 or 3) acute kidney injury (AKI), as an aid in the risk assessment for developing persistent severe AKI (stage 3 AKI lasting ≥ 72 hours) within 48 hours of patient assessment. The VIDAS® NEPHROCLEAR™ CCL14 Test is intended to be used in patients 21 years of age or older. The objective of this study is to determine the reference range for CCL14 concentration in Apparently Healthy Adults and Adults with Chronic, Stable Morbidities
Study Type
OBSERVATIONAL
Enrollment
585
Previously collected urine samples will be tested using the VIDAS® NEPHROCLEAR™ CCL14 Test
George Washington University
Washington D.C., District of Columbia, United States
University of Illinois Chicago
Chicago, Illinois, United States
CCL14 concentration in urine
CCL14 concentration will be measured using the VIDAS Necphroclear CCL14 Assay
Time frame: Samples tested within 2 years of collection
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