Seasonal influenza COVID-19
Conditions
Interventions
None listed
Sponsors
Aillis,Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Persons who have undergone antigen qualitative testing for influenza and novel coronavirus with suspected influenza or COVID-19. 2) Persons aged 6 years or older at the time consent is obtained (however, persons 4 years of age or older may be accepted at pediatric clinics that have received the necessary explanation from Iris Corporation). 3) Persons who have obtained the free written consent of the individual or a surrogate to participate in this study 4) Persons who fall under one or more of the following items from (1) to (4) (however, for items (1) to (3), only persons within 48 hours of the onset of symptoms are counted under the relevant item) (i) Fever of 37.0 C or more (including cases where the temperature exceeded 37 C measured at home, etc.) (ii) With systemic symptoms such as arthralgia, myalgia, headache, or general malaise, anorexia, etc. (iii) Respiratory symptoms with cough, sore throat or nasal discharge/nasal obstruction (iv) Suspected of having influenza or COVID-19 according to a doctor's judgement, such as through concentrated contact with a patient who has influenza or COVID-19
Exclusion criteria
Exclusion criteria: 1) Persons with impaired consciousness or breathing disorders (respiratory failure) 2) Persons with moderate or severe gingival or dental disease or upset teeth that may be aggravated by the use of the research equipment 3) Persons with trauma or damage to the maxillofacial, dental, oral or pharyngeal regions that may be aggravated by the use of the research equipment, or who have undergone surgery on these parts within one month 4) Persons who repeatedly vomit. 5) Persons who have difficulty in taking pictures in a sitting position. 6) Persons who are receiving house calls. 7) Other persons who are judged by the principal investigator or research assistant to be unsuitable as subjects for the study
Countries
Japan
Contacts
Public ContactMemori Fukuda
Aillis,Inc. Clinical Research Promotion Office
Outcome results
None listed