VIDAS Nephroclear (NCL) CCL14 - Sample Stability
Study Details
Study Description
Brief Summary
This VIDAS® NEPHROCLEAR™ CCL14 (VIDAS® NCL™ CCL14) Sample Stability clinical trial is a multicenter, prospective, and qualitative study. The main study objective is to determine sample stability conditions for the VIDAS® NEPHROCLEAR™ CCL14 Test. This 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.
| Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
Product name and intended use
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.
Product description
The VIDAS® NEPHROCLEAR™ CCL14 Test is an automated assay for use on the VIDAS® 3 instrument for the immunoenzymatic quantitative determination of C-C motif chemokine ligand 14 (CCL14) protein in human urine using the Enzyme Linked Fluorescent Assay (ELFA) technique.
Trial Design Overview
This VIDAS® NEPHROCLEAR™CCL14 (VIDAS® NCL™ CCL14) clinical trial is a multicenter, prospective, and qualitative study. 40 to 80 samples collected and tested from subjects enrolled in a related trial will also be tested on the VIDAS® 3 instrument and test.
Trial objectives
The objective of this trial is to identify suitable storage conditions for samples tested using the VIDAS® NCL™ CCL14 for the full measuring range of the assay (0.2 ng/mL to 30 ng/mL). To this end, samples will be tested under the following conditions:
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Fresh, and tested within approximately 2 hours of collection,
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After one freeze-thaw cycle,
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After two freeze-thaw cycles,
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After storage at ambient temperature for approximately 5 hours (tested 5 to 7 hours from collection time), and
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After storage at 2 - 8 ºC for approximately 24 hours (tested 24 to 26 hours from collection time)
Samples collected from at least 40 subjects with urine CCL14 levels spanning the assay measuring range will be analyzed among these conditions.
Study Design
Outcome Measures
Primary Outcome Measures
- Sample stability conditions [one sample will be collected per participant, aliquots will be tested at various conditions: fresh, after one to two freeze-thaw cycles, after refrigeration for 24 hours and after 6 hours at room temperature]
Detection of CCL14 levels in urine, spanning the measuring range of the assay for several sample conditions.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males and females 21 years of age or older;
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Receiving care in an intensive care unit;
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Expected to remain in the ICU for at least 48 hours after enrollment;
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Use of indwelling urinary catheter as standard care at the time of enrollment;
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Subject must have acute kidney injury (KDIGO Stage 2 or Stage 3) at the time of sample collection;
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Urine sample must be collected within 36 hours of meeting KDIGO Stage 2 criteria;
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Written informed consent provided by patient or legally authorized representative (LAR).
Exclusion Criteria:
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Prior kidney transplantation;
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Comfort-measures-only status;
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Already receiving dialysis (either acute or chronic) or in imminent need of dialysis at the time of enrollment;
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Known infection with human immunodeficiency virus (HIV) or active hepatitis (acute or chronic); (NOTE: HIV or hepatitis testing will not be performed for enrollment in this study.)
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Special populations, pregnant women, prisoners or institutionalized individuals;
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | East Carolina University | Greenville | North Carolina | United States | 27834 |
Sponsors and Collaborators
- BioMérieux
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- B3166-CTPR01