Rhinosinusitis Chronic

2

Review clinical trials related to Rhinosinusitis Chronic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

BIOlogics in Severe Nasal POlyposis SurvEy.: a French Registry

With a prevalence of 2-4% in western countries, Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) is of major concern regarding its substantial impact on the social and physical quality of life. So far, endoscopic sinus surgery remains the treatment of choice when the first line of medical treatment with corticosteroid has failed. During the last 15 years, several studies have shown that CRSwNP is associated with a T helper 2 (T2) immune response leading to B cell release of IgE, mucosal recruitment of eosinophils from bone marrow via Interleukin (IL)-5, IL-4 and IL-13 mediated chemoattractant production. New biologic agents capable of blocking T2 cytokines have been developed in the field of eosinophil-associated diseases, shifting the paradigm of treatment for patients with CRSwNP. In the near future, endotype profiling with accurate biomarkers will be mandatory to tailor the treatment of nasal polyposis with specific biologic therapies. Herein the investigators propose a prospective study monitoring medical records of CRSwNP patients who undergo biologic treatments. The objectives are to assess treatment efficacy on quality of life, to report clinical and biological criteria for prescription and to measure tolerance and compliance.Patient-reported outcomes will be addressed according to their initial clinical profile (allergy, asthma, NSAID, gastroesophageal reflux disease, obstructive apnea, otologic disorder, smoke habit).

Participants needed: 900
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, LilleUpdated: May 18, 2026Locations: 2
Eligibility criteria

Patients of over 18-year old requiring a biologic treatment for CRswNP in accord... [+1]

Oral corticotherapy in the previous month; [+5]

Status: Not yet recruiting

Evaluation of the Safety and Performance of a Bioresorbable Nasal Dressing Containing Mometasone Furoate

The objective of this study is to investigate the safety and performance of OCEAN® as an adjunct in wound healing after nasal/sinus surgery by using OCEAN® in patients undergoing nasal/sinus surgery.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Polyganics BVUpdated: Oct 15, 2024
Eligibility criteria

Patient is 18 years or older [+3]

Patient is pregnant or nursing [+13]