Collecting samples from people with respiratory virus infections
Official title: Respiratory Virus Sampling and Repository
Run by National Institutes of Health Clinical Center (CC) · NCT05266222 · Data updated 2026-11-12
This study is collecting blood and nasal samples from people aged 3 and older who have respiratory virus infections to help researchers learn more about these viruses and improve vaccines and treatments.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 3 Years and up |
| Sex | All |
| Enrollment | 20000 (estimated) |
| Sponsor | National Institutes of Health Clinical Center (CC) NIH |
| Locations | 2 sites (Bethesda, Maryland and 1 other locations) |
| Status | Recruiting |
| Started | August 11, 2022 |
| Main results expected | December 31, 2031 |
| Study ends | December 31, 2031 |
| Registry record updated | August 17, 2026 |
| Trial ID | NCT05266222 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals aged 3 and older with documented or suspected respiratory virus infections.
✕Probably not a fit
Patients who do not have a respiratory virus infection or have conditions that compromise their safety may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to gather samples from individuals aged 3 and older who have or are suspected to have respiratory virus infections, such as influenza and COVID-19. Participants will provide blood and nasal samples, and data from their medical records will be collected. The samples will be used to study respiratory viruses and the immune responses to them, contributing to future research on vaccines and treatments. The study will take place over a duration of 10 years at the NIH Clinical Center.
Why it matters
Potential benefit: If successful, this study could enhance our understanding of respiratory viruses and improve future vaccine and treatment development.
How similar studies have gone: Other studies have successfully collected respiratory virus samples for research, indicating that this approach is viable and beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
* INCLUSION CRITERIA: In order to be eligible to participate in this study, an individual must meet all of the following criteria: 1. Aged 3 years or older. 2. Documented or suspected infection with a respiratory virus. 3. Stated willingness to comply with all study procedures for the duration of the study. EXCLUSION CRITERIA: An individual who meets any of the following criteria will be excluded from participation in this study: 1\. Any condition that, in the opinion of the investigator, would compromise the safety of the study participant or staff, or would prevent proper conduct of the study. Non-English Speaking Participants: This study will enroll non-English speaking participants. For non-English speaking participants, the study will be explained to the participant/family through an interpreter, in the presence of the study team, in the language understood by the participant/family. The short form in the language understood by the participant/family will be signed by the participant/family or LAR and the interpreter, and the consent will be signed by the consenting provider and the interpreter.
Where it's running
-
National Institutes of Health Clinical Center
Bethesda, Maryland, United States Recruiting -
NIH Building 33 (NIAID)
Bethesda, Maryland, United States Recruiting
Study contacts
- Principal investigator: Matthew J Memoli, M.D. — National Institute of Allergy and Infectious Diseases (NIAID)
- Study coordinator: Rani S Athota, Ph.D.
- Email: rani.athota@nih.gov
- Phone: (301) 594-0803
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Comparative Immunogenicity of Respiratory Virus Vaccines (CIRV2) in Adults
This study tests and compares the immune responses and tolerability of the latest COVID-19 vaccines from Novavax and Pfizer/BioNTech in adults at risk for severe COVID-19.
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Virological Monitoring of Seasonal Respiratory Infections in France
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This small, year-long study tests how brain activity and smell-related inflammation relate to different smell disorders in adults.
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Monitoring and detection of influenza, RSV, and COVID-19 in adults with and without HIV in Lusaka
This project will test methods to detect influenza, RSV, and COVID-19 in adults with and without HIV who have recent respiratory symptoms in Lusaka.
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Evaluating COVID-19 and influenza vaccine schedules for immunocompromised individuals
This study is testing different ways to give COVID-19 and flu vaccines to people with weakened immune systems to see which method works best for their protection.
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A program to empower community health workers to combat vaccine misinformation
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.