Evaluation of Treatments for Sore Throat Associated With Acute Pharyngitis and/or Viral Tonsillitis

Recruiting N/A Interventional Study
Acute Pharyngitis Viral Sore Throat
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
160 (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: HMG, PHN, PHR, and TUR. 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 sore throats related to acute pharyngitis and/or viral-origin tonsillitis, while also assessing the benefit/ris…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Pharyngitis or tonsillitis or acute nasopharyngitis or viral-origin sore throat with odynophagia that began less than 72 hours before the inclusion visit according to the investigator's judgment * Bacterial rhinopharyngitis with negative TROD test * Effective contraception for…
Contacts

Lise Laclautre

+33473754963

promo_interne_drci@chu-clermontferrand.fr

CONTACT