Development of a minimally invasive, ultra-sensitive rapid diagnosis kit for influenza virus

Development of a minimally invasive, ultra-sensitive rapid diagnosis kit for influenza virus - Development of rapid diagnosis kit for influenza virus

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000038997

Enrollment

400

Registered

2020-05-31

Start date

2019-12-11

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 infection

Interventions

Sampling of oral mucosa, pharyngeal abrasion, nasopharyngeal swabs, nasal discharge, and saliva of patients and healthy people with dense contact

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients visited for complaints of influenza-like symptoms in an influenza virus infection endemic area, and its rich contact healthy people

Exclusion criteria

Exclusion criteria: nothing

Design outcomes

Primary

Measure	Time frame
Diagnostic accuracy for each specimen collection site and test method	—

Secondary

Measure	Time frame
Onset threshold of influenza virus infection	—

Countries

Japan

Contacts

Public ContactHironobu Kamagata

University of Tokyo Noji Laboratory, Department of Applied Chemistry

kamagatahrn1981@gmail.com03-5841-1872

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026