The objective of this study is to demonstrate the clinical performance of the Sofia® 2 analyzer and Sofia Lyme FIA test in the CLIA waived test environment in comparison to Comparator Method(s) and/or an FDA cleared predicate test(s) using matched finger-stick, whole blood and serum from symptomatic subjects.
The objective of this study is to demonstrate the clinical performance of the Sofia® 2 analyzer and Sofia Lyme FIA test in the CLIA waived test environment in comparison to Comparator Method(s) and/or an FDA cleared predicate test(s) using matched finger-stick, whole blood and serum from symptomatic subjects. The finger-stick and venous whole blood specimens will be tested by CLIA waived test operators. The matched plasma (from the leftover whole blood) and serum specimens will be sent to a separate reference laboratory for testing to compare the matched specimen using the Comparator Method(s) and/or an FDA-cleared predicate test(s). The results of this study may be used to support a 510(k) and/or CLIA-Waiver submission for testing whole blood sample types.
Study Type
OBSERVATIONAL
Enrollment
597
IVD testing of whole blood or serum/plasma to aid in the detection of anti-B. burgdorferi IgG / IgM antibody
NECCR Primacare Research, LLC
Fall River, Massachusetts, United States
Main Road Family Medicine
South Westport, Massachusetts, United States
Essentia Institute of Rural Health
Duluth, Minnesota, United States
Detection of anti-B. burgdorferi IgG / IgM antibody
Accurate detection of presence or absence of anti-B. burgdorferi IgG / IgM antibody
Time frame: 15 minutes
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