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Reproducibility and Method Comparison Studies of the Quo-Test™ A1C System and the Quo-Lab A1C Test and CLIA Waiver Study of the Quo-Test™ A1C System

Diabetes Clinical Trial

Official title:
Reproducibility and Method Comparison of the Quo-Test™ A1C System and the Quo-Lab A1C Test and CLIA Waiver of the Quo-Test™ A1C System

Clinical Trial Summary

The Quo-Test A1C Analyzer and Reagent Test System (Quo-Test A1C System) are intended for the in-vitro quantitative determination of glycated hemoglobin in whole blood samples obtained from fingerstick or venous samples for point-of-care testing. The Quo-Test A1C System is indicated in the management and treatment of diabetes and for monitoring long term glycemic control by diabetics. It is for multiple patient use. Only auto-disabling, single use lancing devices should be used with this system.

Clinical Trial Description

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Study Design

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Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01829061
Study type Observational
Source Quotient Diagnostics Limited
Contact
Status Terminated
Phase N/A
Start date April 2013
Completion date April 2014
View Details
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