New 3-in-1 test for COVID, flu, and RSV put to the test
NCT ID NCT06689423
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study checked how well a new test called VitaSIRO solo™ detects COVID-19, flu, and RSV in people with respiratory symptoms. Over 1,200 participants provided nose and throat swabs. The test's accuracy was compared to standard lab methods.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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1,268 people
The number who actually took part.
- Started
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Nov 2024
- Finished
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Dec 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Subjects involved in the study include individuals displaying signs and/or symptoms of respiratory tract infections as per the intended purpose of the VitaSIRO solo™ SARS-CoV-2/Flu/RSV Assay. There are no specifications for subjects based on age, race, sex or any other demographic. However, demographic information will be collected for each subject.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject displaying one or more of the following signs and/or symptoms of a respiratory tract infection: 1. Fever 2. Cough 3. Nasal Congestion 4. Shortness of breath 5. Difficulty in breathing 6. Runny nose 7. Sore throat 8. Muscle pain 9. Headache 10. Chills 11. Nausea 12. Diarrhoea 13. Vomiting 14. New loss of taste/smell * If age 18 or over, subject is willing and capable of providing written informed consent. If under the age of 18, parent or legal guardian is willing to and capable of providing consent/assent. Assent should be obtained from minor subjects of appropriate intellectual age as defined by the IRB. Exclusion Criteria: * Subject is unable to provide consent and assent (as appropriate) or parental/legal guardian consent permission and assent (as appropriate) cannot be obtained. * PI determines that specimen collection represents an unacceptable risk. * Subjects who have already been enrolled in the study previously.
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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.
Contacts and locations
Locations
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Credo Diagnostics Biomedical Pte Ltd. Taiwan Branch
New Taipei City, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can an oral drug stop COVID-19 from turning deadly?