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It is a rapid qualitative test for detection Trichomonas vaginalis.
Principle:
Color immunochromatography, capillary flow dipstick assay detecting pathogen antigens directly from vaginal swabs
- Quality check:
Provides two methods of control for the assay: internal controls to aid in determining test validity, and external controls to demonstrate proper test function.
- Rapid
Results are ready in 10 minutes.
- Accuracy:
83% sensitive and 99% specific as compared to reference culture
95% agreement against composite standard reference methods
- Certification:
US FDA approved and CLIA waived.
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