Treatments for sore throat linked to acute pharyngitis and viral tonsillitis

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study collects real-world clinical data to monitor the tolerance, safety, and efficacy of four medical devices used for sore throat related to acute pharyngitis and viral-origin tonsillitis. It is an observational, post-marketing follow-up rather than a randomized trial. Participants must have sore throat with onset within 72 hours and meet specific inclusion criteria, while excluding those with certain infections or allergies. Data are gathered in routine clinical settings to assess risk/benefit in typical use. The lead sponsor is University Hospital, Clermont-Ferrand, with participation at Chu Clermont Ferrand in Clermont-Ferrand, France.

Why it matters

Who can join: the full rules

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 female patients of childbearing age
* Cooperation and sufficient understanding to comply with the requirements of the trial
* Acceptance of registration in the SI-RIPH database
* Having received informed information and agreeing to give written consent
* Affiliated with the French Social Security scheme.

Exclusion Criteria:

* Hypersensitivity/previous allergy to any of the product components,
* Pharyngitis or tonsillitis or acute rhinopharyngitis complicated (phlegmon, acute otitis media, pneumonia…) or severely intolerable cough,
* Positive antigen test for influenza A/B or COVID-19 and infection requiring etiological treatment according to the recommendations,
* Other ongoing treatments for acute pharyngitis or tonsillitis (local treatment, antibiotics, corticosteroids, antiretroviral…),
* Comorbidities or health conditions deemed incompatible with the trial by the investigator,
* Recent otorhinolaryngology surgery (\<6 months),
* Pulmonary pathology (Chronic Obstructive Pulmonary Disease, asthma…),
* Immunosuppression (according to patient's report),
* Pregnant or breastfeeding women,
* Currently participating in another clinical trial, or in the exclusion period, or having received total compensation of more than €6,000 in the 12 months prior to the start of the trial,
* Benefiting from legal protection measures (guardianship, trusteeship, deprivation of liberty, judicial protection).

Where it's running

• Chu Clermont Ferrand
  Clermont-Ferrand, France Recruiting

Study contacts

• Study coordinator: Lise Laclautre
• Email: promo_interne_drci@chu-clermontferrand.fr
• Phone: +33473754963

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.