Influenza Clinical Trial
Official title:
Clinical Validation of the Respirio Flu Test for the Rapid Identification of Influenza A/B in the Primary Health Setting
This is a open label, prospective, pair comparison, randomised, multi-centre trial. The
primary aim of this study to is to clinically validate the sensitivity and specificity of
the Respirio Flu Test (RFT) in detecting Influenza A as compared with (a) the best available
rapid Influenza A test in the market Quidel QuickVue (QQV) and (b) the gold standard for
identifying Influenza A infection Polymerase Chain Reaction (PCR).
The secondary aim is to clinically validate the sensitivity and specificity of the Respirio
Flu Test (RFT) in detecting Influenza B as compared to QQV and PCR.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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