Comparison of detection sensibility of various specimen collection methods for respiratory infectious pathogens, and Gene sequence analysis of viral pathogens.

Comparison of detection sensibility of various specimen collection methods for respiratory infectious pathogens, and Gene sequence analysis of viral pathogens. - Comparison of detection sensibility of various specimen collection methods for respiratory infectious pathogens, and Gene sequence analysis of viral pathogens.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000050254

Enrollment

100

Registered

2023-02-07

Start date

2023-02-16

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

none

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Subjects who gave written informed consent to participate in the trial. 2)Japanese women and men aged 50 years or older. 3)Subjects who have at least any one of the symptoms of common cold that occurred within 72 hours before the subject visit to the study site at the time of informed consent. The symptoms of common cold are: Nasal discharge, nasal congestion, pharyngitis, cough, wheezing, phlegm, shortness of breath, or body temperature of 37.5 C or higher.

Exclusion criteria

Exclusion criteria: Subjects who were considered by the investigator or subinvestigator to be ineligible for the participant in the trial.

Design outcomes

Primary

Measure	Time frame
Detection sensibility in various specimen collection methods and gene sequence analysis.	—

Countries

Japan

Contacts

Public ContactHidetoshi Furuie

Medical Corporation Heishinkai OPHAC Hospital none

hidetoshi.furuie@heishinkai.com06-6395-9000

Outcome results