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RECRUITINGINTERVENTIONAL

RSV Burden in Outpatient and Hospital Settings

Ambulatory Respiratory Tract Infection Survey, Burden of Respiratory Syncitial Virus in the Era of Covid-19

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Strengthening outpatient low respiratory tract infection surveillance to document the burden of Respiratory Syncytial Virus (RSV)

Who May Be Eligible (Plain English)

Who May Qualify: - children under 24 months of age (≤) - One of the holders of parental authority signed the consent - Patient affiliated to a social security scheme (Social Security or Universal Medical Coverage) - Acute purulent otitis media (Paradise Criteria) or otorrhea with or withitout associated bronchiolitis Who Should NOT Join This Trial: - Age \>24 months - Refusal by one of the parents - Not affiliated to a social security system - Maternal RSV vaccination during the pregnancy of the included child Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * children under 24 months of age (≤) * One of the holders of parental authority signed the consent * Patient affiliated to a social security scheme (Social Security or Universal Medical Coverage) * Acute purulent otitis media (Paradise Criteria) or otorrhea with or withitout associated bronchiolitis Exclusion Criteria: * Age \>24 months * Refusal by one of the parents * Not affiliated to a social security system * Maternal RSV vaccination during the pregnancy of the included child

Treatments Being Tested

DIAGNOSTIC_TEST

nasopharyngeal samples

rapid antigen test for Sars Cov-2, influenza and RSV.

Locations (1)

ACTIV
Créteil, France