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Clinical Trials/JPRN-UMIN000037891
JPRN-UMIN000037891
Completed
未知

A Prospective Epidemiology Study to Estimate the Attack Rate of Respiratory Syncytial Virus Infection in Adults Aged 65 Years and Older in Japan - A Prospective Epidemiology Study to Estimate the Attack Rate of Respiratory Syncytial Virus Infection in Adults Aged 65 Years and Older in Japan

Janssen Pharmaceutical K.K. R&D Clinical Science div. Infectious disease & Vaccine Clinical Development Dept.0 sites1,000 target enrollmentSeptember 2, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Respiratory Syncytial Virus Infections
Sponsor
Janssen Pharmaceutical K.K. R&D Clinical Science div. Infectious disease & Vaccine Clinical Development Dept.
Enrollment
1000
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Respiratory syncytial virus was reported as a major pathogen for respiratory infection and represents a significant burden in the Japanese elderly population.

Registry
who.int
Start Date
September 2, 2019
End Date
July 6, 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Janssen Pharmaceutical K.K. R&D Clinical Science div. Infectious disease & Vaccine Clinical Development Dept.

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • \-Participants received any experimental antiviral drugs or vaccines against respiratory syncytial virus (RSV) within 6 months prior to the signing Informed Consent Form (ICFs) \- Participants who have acute respiratory disease (ARD) at the time of ICF and Week 0 (Baseline) at the discretion of the investigator \- Participants with life expectancy less than 1 year \- Participants unwilling to undergo nasopharyngeal swab procedures or with any physical abnormality which limits the ability to collect regular nasopharyngeal specimens \- Participant who is not able to comply with study\-related procedures,due to their mental status or severe clinical condition, based on clinical judgement of the investigator

Outcomes

Primary Outcomes

Not specified

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