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Clinical Trial Summary

In this study, investigators evaluated for the first time the diagnostic efficacy of abioSCOPE® versus Phadia Laboratory System as an aid in the diagnosis of allergic diseases. Investigators targetted the agreement between test results obtained in abioSCOPE® and a laboratory reference method (Phadia Laboratory System, ThermoFisher Scientific, Uppsala, Sweden), considered as a quasi-gold standard in IgE (immunoglobulin E) antibody assays. Investigators also reported the medical decision taken by a panel of allergy experts who had access to patient history, skin tests and IgE antibody assay, but blinded to the method used, i,e, the reference method or the abioSCOPE® .


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03599908
Study type Observational
Source Centre Hospitalier Universitaire Vaudois
Contact
Status Completed
Phase
Start date January 2013
Completion date December 21, 2016

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