About this trial
The purpose of this research study to understand how prior respiratory infections affect the susceptibility to lung inflammation following environmental exposures.
Eligibility criteria
Qualifiers
Individuals between 18-55 yrs. of age (No subject will be excluded from the study on the basis of gender or ethnicity)
Individuals with knowledge of prior respiratory viral infection history allowing them to be segregated into one of three cohorts
Cohort 1 - No history of respiratory viral infection (defined as no symptoms consistent with respiratory viral infection nor history of a positive respiratory viral test)
Cohort 2 - Documented mild respiratory viral infection (a positive test, either PCR- or antigen-based) but with mild to no symptoms and no evidence of a lower respiratory tract infection (including no hospitalization, and no oxygen use)
Disqualifiers
Individuals with prior respiratory viral pneumonia who have ongoing respiratory symptoms, are still using supplemental oxygen, or have abnormal lung function
Current smokers of tobacco products including e-cigarettes or those with previous smoking history within the prior 5 years
Pregnant women and women who are presently lactating.
Subjects that have received antibiotic administration or an upper respiratory infection within the previous 4 weeks
Trial design
Treatments tested in this trial
- Ozone
Treatment groups
Sponsors and collaborators
Robert Tighe, MD
Lead sponsor
Duke University
Sponsor institution
National Institutes of Health (NIH)
Collaborator
National Institute of Environmental Health Sciences (NIEHS)
Collaborator