Epidemiologic study;Efficacy study of new diagnosis kit (rapid antigen test) for influenza virus in early diagnosis. An open-label, non-randomized, multi-central study.

Epidemiologic study;Efficacy study of new diagnosis kit (rapid antigen test) for influenza virus in early diagnosis. An open-label, non-randomized, multi-central study. - KS-BF study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000010032

Enrollment

100

Registered

2013-02-14

Start date

2013-02-09

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

Influenza virus infections.

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Target information. 1) Gender: Male or female. Age: over 28 days old. 2) Bellow data; a)Duration of influenza. b)Use Brightpoc TM-Flu for diagnosis. c)Judgment result of Brightpoc(TM)-Flu (negative-positive, virus sub-type). d)Virus isolation and PCR. 3) The patients with agreement.

Exclusion criteria

Exclusion criteria: Non target information. Patients who are deemed to be inappropriate by the investigator.

Design outcomes

Primary

Measure	Time frame
The positive rate of Brightpoc(TM)-Flu according to duration of influenza infection.	—

Countries

Japan

Outcome results