Influenza infection
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Among the patients registered in the Influenza Follicle Data Collection Research, we have been able to obtain information on the following Patient characteristics Physical findings, subjective symptoms Clinical test information 2.Those determined to be influenza positive by PCR method
Exclusion criteria
Exclusion criteria: Cases in which information regarding patient characteristics, physical findings, subjective symptoms, and clinical test information cannot be obtained.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint: (1) Relationship between body temperature and Ct value at the time of visit | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints (2) Relationship between the presence or absence of subjective symptoms at the time of visit and Ct value (3) Relationship between the number of subjective symptoms at the time of visit and Ct value Exploratory evaluation items (4) Relationship between time from onset of symptoms to hospital visit and subjective symptoms at hospital visit (5) Relationship between Ct value at visit and vaccination history (6) Relationship between body temperature at the time of visit and vaccination history | — |
Countries
Japan
Contacts
Aillis, Inc. Research & Collaboration