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Comparison of the ID NOW and Accula Point-of-Care Assays for Detection of COVID-19
Comparison of the ID NOW and Accula Point-of-Care Assays for Detection of COVID-19
WithdrawnN/A
Sponsor: Henry Ford Health System
Conditions: Covid-19
Interventions: ID NOW vs. Accula
Countries: United States
This study is a comparison of the ID Now COVID-19 (Abbott) assay to the Accula SARS-CoV-2 (Mesa Biotech) assay to assist in the identification of infection with COVID-19. The tests will be compared for sensitivity, specificity, positive predictive value and negative predictive value.
Eligibility overview
Sex: ALL
Age: 18 Years to 95 Years
Study type: OBSERVATIONAL
Eligibility criteria
Inclusion Criteria: * Covid-19 testing has been ordered in the Emergency Dept. or for inpatients in the hospital or patient has already tested positive via PCR. * Adult patients * Consent obtained Exclusion Criteria: * Testing not ordered or tested negative via PCR. * Children * Do not consent
Locations (1)
- Detroit, Michigan, United States