RhinAV_Evaluation of Treatments for Acute Viral Rhinitis, Rhinosinusitis, and Rhinopharyngitis

Recruiting N/A Interventional Study
Rhinitis Acute Rhinitis Viral Rhinosinusitis Acute Rhinopharyngitis Rhinitis Rhinosinusitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 70
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
150 (estimated)
Sponsor
University Hospital, Clermont-Ferrand · Other
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About This Trial
The objective of this study is to conduct post-marketing clinical follow-up of four products: NS, NHE, NHG, and PIR. This follow-up will consist of collecting clinical data in real-life conditions to confirm the tolerance, safety, and efficacy of medical devices used in the treatment of acute viral rhinitis, rhinosinusitis, and rhinopharyngitis, while also assessing the benefit/risk ratio of the p…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Acute viral rhinitis or acute rhinosinusitis or viral rhinopharyngitis (sneezing, rhinorrhea, nasal obstruction, cough secondary to posterior rhinorrhea, sore throat) that began less than 72 hours prior to the inclusion visit, in the investigator's judgment, * Effective contra…
Contacts

Lise Laclautre

+33473754963

promo_interne_drci@chu-clermontferrand.fr

CONTACT

Lise Laclautre

CONTACT