FLU A+B Nasal Swab Clinical Study
Completed
Conditions studied: Influenza
In brief
The purpose of this clinical study is to obtain clearance for the nasal swab sample type by demonstrating the performance characteristics of the FLU A+B Test versus standard laboratory culture for Influenza A and B viruses using nasal swab samples.
Key facts
- Study ID
- NCT00636662
- Run by
- Response Biomedical Corp.
- People needed
- 800
- Starts
- 2008-02-01
- Expected to finish
- 2008-05-01
- Last updated by the study team
- 2019-03-27
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male and Female of all age groups
- Patients exhibiting influenza symptoms (i.e., fever, body aches, headaches, cough, sore throat, and other respiratory symptoms) at the time of examination
- Patients must either present with a fever (>100ºF; >37.8ºC) at time of examination or have had a fever (>100ºF; >37.8ºC) or declare at time of the examination that they had a fever within the previous 3 days prior to the examination
- Must be able to collect sample using the nasal swab sample type
You may not qualify if…
- Patients with no fever at time of examination or within the 3 days prior to examination and/or are currently undergoing treatment (including anti-virals) will be excluded from the study.
Where it is running
- Northwestern University — Chicago, Illinois, United States
- Washington University / St. Louis Children's Hospital — St Louis, Missouri, United States
- Wake Forest University Health Sciences — Winston-Salem, North Carolina, United States
- Dell Children's Hospital — Austin, Texas, United States
- Mt. Sinai Hospital — Toronto, Ontario, Canada
Full record on ClinicalTrials.gov
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