COVID Clinical Trial
Official title:
A Human Clinical Study to Collect Calibration and Performance Data for the RBA-2 Device
The current available diagnostic methods used for the detection of COVID-19 takes up to 4 hours. In some cases, these diagnostics tests make take up to a couple of days. As it is highly contagious, people who are in close contact with the infected person are at high risk of being infected. COVID-19 is transmitted through respiratory droplets produced when an infected person coughs or sneezes. The desire for rapid detection of COVID-19 has become an immediate necessity. The purpose of Kaligia Biosciences' saliva monitoring device (RBA-2) is to detect the presence of the COVID-19 virus in human saliva. The RBA-2 uses Raman Spectros-copy to detect the coronavirus. Once the sample is scanned successfully, the spectra contains the response of the component present in human saliva and provide results in a matter of minutes, rather than hours or days.
The purpose of this study is to calibrate the performance of RBA-2 using people by comparing
the results against a standard diagnostics test. The objective of this study is to collect
non-invasive in vivo saliva from confirmed cases of both infected and non-infected COVID-19
patients or site staff at the testing site and compare the test results using the RBA-2
against the standard test results used for diagnosis.
The comparison of the results obtained from the current testing methods will be used to
calibrate machine learning algorithms of the RBA-2.
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