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Prospective Study in Respiratory Syncytial Virus Infected Japanese Adults, in Outpatient and Inpatient Settings

Not Applicable
Conditions
acute respiratory infection
Registration Number
JPRN-UMIN000019120
Lead Sponsor
Janssen Pharmaceutica NV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

1.Patient participates in another clinical study, with the exception of registry and epidemiology studies, involving minimum sampling done prior to the patient screening for the proposed study. 2.Patient is not able to provide informed consent prior to any study-related procedure(s), due to the mental status or severe clinical condition. 3.Patient has known dementia. 4.The onset of the acute respiratory symptoms was >7 days ago.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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