Clinical Evaluation of a COVID-19 Antigen Self-Test (CoviDx™)

Stopped early

Conditions studied: SARS-CoV-2, Covid19

In brief

Prospective study that will evaluate the clinical agreement of the CoviDx™ Self test compared to SARS-CoV-2 RT-PCR.

Key facts

Study ID

NCT05403346

Run by

Lumos Diagnostics

People needed

45

Starts

2022-05-17

Expected to finish

2022-10-31

Last updated by the study team

2022-11-16

Who can join

Age: 2 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Mid-turbinate nasal swab collected for SARS-CoV-2 RT-PCR at the same time of CoviDx Rapid Antigen swab collection
• Symptomatic subjects suspected of having COVID-19, first onset of COVID-19-like symptoms (e.g., chills, cough, shortness of breath or difficulty breathing, fatigue, muscle or body aches, headache, new loss of taste or smell, sore throat, congestion or runny nose, nausea or vomiting, or diarrhea) should not have started more than 5 days from the time of the study visit. Symptoms must be present on the day of CoviDx testing.
• ≥ 2 years of age
• Participants between 2-13 years of age, inclusive, must participate with a guardian who will be collecting the swab.
• Signed Informed Consent

You may not qualify if…

• Participants with prior medical or laboratory training
• Unable or unwilling to provide signed, Informed Consent
• Less than 2 years of age
• Received a positive diagnostic test result for COVID-19 in the past 14 days
• Received a negative diagnostic test result for COVID-19 in the last 18 hours
• Study Comparator collection that occurred > 3 hours from CoviDx swab collection
• For symptomatic participants: first onset of COVID-19-like symptoms occurring more than 5 days from study visit
• Invalid or missing study comparator test results
• Use of a non-high-sensitive SARS-CoV-2 test as the comparator SARS-CoV-2 RT-PCR test (e.g., rapid molecular, rapid antigen tests, tests that do not have FDA EUA, a test that was not approved by Sponsor for use in the study)
• Enrollment in another study involving the collection of a nasopharyngeal, mid-turbinate nasal swab or anterior nasal swab within 6 hours of CoviDx testing.
• Indicates they would not use a COVID-19 diagnostic test kit in real life
• Taking any of the following medications or treatments within 7 days of study visit (antivirals (e.g., Remdesivir, Paxlovid) and/or monoclonal antibodies (e.g., REGEN-COV (casirivimab, imdevimab), Sotrovimab (Xevudy), Evusheld)
• Nasal spray administration in the last 48 hours

Where it is running

• PAS Research — Tampa, Florida, United States

Full record on ClinicalTrials.gov

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