Evaluation of clinical trial for the rapid detection kit of Respiratory Syncytial Virus

Evaluation of clinical trial for the rapid detection kit of Respiratory Syncytial Virus - Evaluation of clinical trial for the rapid detection kit of RSV

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000020312

Enrollment

400

Registered

2015-12-22

Start date

2013-09-01

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

RSV infections

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who come to the institutions and are applicable to the following items 1) Patients who have lower respiratory tract inflammation with suspicion of RSV 2) Patients who have agreed with the participation to this clinical trial

Exclusion criteria

Exclusion criteria: 1) Patients who have difficulty to collect Specimens 2) An investigator determines that a patient is unsuitable for this study

Design outcomes

Primary

Measure	Time frame
Positive, negative and total concordance rate in comparison with the RT-PCR method	—

Countries

Japan

Contacts

Public ContactAtsuko Shinozaki

Eiken Chemical Co.,Ltd. Biochemical Research Laboratory-I

Atsuko_Shinozaki@eiken.co.jp0280-57-0715

Outcome results