Data collection clinical studies, including pharyngeal imaging, in patients with seasonal influenza or COVID-19

Data collection clinical studies, including pharyngeal imaging, in patients with seasonal influenza or COVID-19 - Data collection clinical studies, regarding influenza or COVID-19

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000052896

Enrollment

4600

Registered

2023-12-01

Start date

2023-12-22

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Seasonal influenza COVID-19

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who present to the outpatient clinic of the Principal Investigator or Co-Investigator (excluding Aillis, Inc.) with complaints of fever and airway symptoms and who fulfil all of the following 1), 2), 3) and 4) will be included in the study. If the patient is seen again with similar symptoms during the study period, he/she may be enrolled in the study again. 1) Persons who have undergone antigen qualitative testing for influenza and novel coronavirus with suspected influenza or COVID-19. 2) Persons aged 4 years or older at the time consent is obtained 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) Other persons who are judged by the principal investigator or research assistant to be unsuitable as subjects for the study

Design outcomes

Primary

Measure	Time frame
-	—

Countries

Japan

Contacts

Public ContactMemori Fukuda

Aillis,Inc. -

clinicalresearch_flucov2023_01@aillis.jp03-5218-2374

Outcome results