Coronavirus Infections, COVID-19
Conditions
Brief summary
This prospective clinical performance study is a non-interventional, multi-center study to evaluate the assay performance of the COVID-19 test using upper respiratory specimens. Prospectively collected nasopharyngeal and anterior nasal swabs will be collected from each participant recruited in the study.
Detailed description
The Applied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit (referred to as COVID-19 test) aims to develop a reverse transcription, real-time polymerase chain reaction (RT-qPCR) test for the qualitative detection of SARS-CoV-2. The purpose of this study is to evaluate the clinical performance of the TaqPath™ COVID-19 Diagnostic PCR Kit (COVID-19 test) in nasopharyngeal swabs and anterior nasal swabs from symptomatic individuals suspected of COVID-19 by their health care provider. A composite comparator approach will be used to evaluate the performance of the COVID-19 test which includes the use of three highly sensitive SARS-CoV-2 molecular assays as comparators. Clinical calls will be compared between COVID-19 test and the three composite comparators. The third comparator assay will only be used to test samples that show discrepant clinical calls between the first two comparator methods, for a two-out-of-three result interpretation. The Clinical Performance Study Protocol (CPS Protocol) outlines the clinical sample collection and testing protocols which will be used to satisfy the FDA 510(k) study requirements in the US.
Interventions
DIAGNOSTIC_TESTApplied Biosystems™ TaqPath™ COVID-19 Diagnostic PCR Kit
A reverse transcription, real-time polymerase chain reaction (RT-qPCR) test for the qualitative detection of SARS-CoV-2.
Sponsors
Thermo Fisher Scientific, Inc
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
Participants of all ages must meet the following inclusion criteria to be eligible for participation in the study: * Ability to provide informed consent or assent (as age-appropriate). Stated willingness and ability to comply with the study procedures including nasopharyngeal and anterior nasal swab collection. * Individuals with at least one of the following COVID-19 symptoms: 1. fever or chills 2. congestion or runny nose 3. headache or fatigue 4. muscle or body aches b. new loss of taste or smell c. a new or worsening cough or sore throat d. shortness of breath or difficulty breathing e. decrease in appetite, nausea, vomiting, diarrhea. * Subjects suspected of having COVID-19 symptoms for seven (7) or fewer days.
Exclusion criteria
Participants meeting the following criterion will be excluded from the study: * Subjects suspected of having COVID-19 symptoms for greater than seven (7) days. * Subjects who have provided upper respiratory tract samples for other clinical studies within twenty-four (24) hours
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical performance evaluation of the COVID-19 test | Between April 2023 and August 2023 | Clinical performance evaluation of the COVID-19 test using a composite comparator approach with upper respiratory specimens to meet PPA and NPA requirements. |
| Identification of adverse events | Between April 2023 and August 2023 | Identify any adverse events or complications associated with the COVID-19 test |
Countries
United States
Outcome results
None listed