Rapid COVID test vs. gold standard: study aimed to see if cheap antigen tests work for contact tracing
NCT ID NCT04745533
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to compare a rapid antigen detection test against the standard PCR test for diagnosing COVID-19 in people who were close contacts of infected patients but had no symptoms. The goal was to see if the quick, inexpensive antigen test could reliably identify contagious individuals during quarantine. However, the study was withdrawn before enrolling any participants, so no data were collected.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Antigen detection test (rapid diagnostic test)
- What this could lead to
- If successful, this could show that cheap, rapid antigen tests are reliable for screening asymptomatic contacts, helping to quickly identify contagious people and slow virus spread.
- What could go wrong
- The study was withdrawn before any participants were enrolled, so no results are available. Antigen tests are less sensitive than PCR, especially in people without symptoms, so they might miss some infections.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Started
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Feb 2021
- Finished
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Jun 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
All subjects considered close contacts of COVID-19 patients according to the definition of the Ministry of Health of Spain in the health area of Cáceres
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects considered close contacts of COVID-19 patients according to the definition of the Ministry of Health of Spain at the time of inclusion. Exclusion Criteria: * Subjects who do not obtain their informed consent for the study. * Symptomatic subject at the time of inclusion.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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