Seasonal Influenza Study

Updated on 23 November 2020


Seasonal Influenza Study


A Study for patients with Seasonal Influenza.

Patients may receive up to $150 for time and travel.

Condition Influenza
Clinical Study IdentifierTX143088
Last Modified on23 November 2020


Yes No Not Sure

Inclusion Criteria

Patients must come to clinic with symptoms suggestive of a diagnosis of acute influenza. Must have documented oral temperature of 100.4°F at any time during screening. Must also have at least one “moderate” respiratory symptom (cough, sore throat, nasal stuffiness) and at least one “moderate” systemic symptom (headache, muscle or joint pain, feverishness [feverishness or chills], fatigue). Time of onset of influenza-like symptoms to anticipated start time of treatment must be ≤48 hours. Onset of symptoms is (within 1 hour) of when the subject becomes aware of respiratory or systemic symptoms and experiences an oral temperature of 100.4°F. Must also have positive test for influenza type A. If patients had intranasal spray vaccine (e.g., Flumist®) in the 3 weeks before study entry they are excluded. Patients taking any antiviral medications in the last 14 days are excluded
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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