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Anatomo-clinico-biological Profiles in Severe Nasal Polyps

Not Applicable
Recruiting
Conditions
NASAL POLYPS
Interventions
Other: identification anatomo-clinico-biological profiles
Registration Number
NCT06362122
Lead Sponsor
Poitiers University Hospital
Brief Summary

Nasal sinus polyposis is a chronic inflammatory pathology of the nasal cavity and sinus cavities that causes bilateral and multifocal polyp development and has a prevalence of 2 to 4% in the general population.

Therapeutic management consists of first-line medical treatment for anti-inflammatory purposes. Local corticosteroid therapy, using nasal sprays, is the background treatment. Surgical management is offered to patients in case of failure of medical treatment. Although effective, surgery does not protect patients from recurrence of symptoms related to regrowth of polyps. Recently, biologics have appeared, which despite its effectiveness, about 20% of patients have a partial or no response to these treatments. There is currently no possibility of determining the probability of response to treatments in patients.

It is therefore essential to determine an anatomo-clinico-biological correlation associating the anatomopathological profile, the clinical characteristics and the cytokine signature in order to best guide the patient's management, including the initiation of biotherapy. Indeed, patients, according to their clinical, biological characteristics and the cytokine signature of their polyps will react differently to different treatments, including surgery and biotherapy. This correlation will serve as a predictor of treatment response.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Patient ≥ 18 year-old
  • Patient with nasal sinus polyposis resistant to medical treatment and requiring surgical treatment with ethmoidectomy type is considered for the first time
  • Having signed the consent form
  • Having an health insurance
Exclusion Criteria
  • Current or past biotherapy treatment
  • Taking general corticosteroid therapy within 4 weeks of surgery
  • Protected person
  • Pregnant women or lactating women

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
patients with nasal polypsidentification anatomo-clinico-biological profiles-
Primary Outcome Measures
NameTimeMethod
Evaluation of symptoms related to nasal sinus polyposis by visual analogue scale1 day

the measurement by the visual analogue scale (ranging from 0 (no) to 10 (very intense)

Identify anatomical profiles present in nasal sinus polyposis resistant to medical treatment.1 day

Caracterization the profiles of patients by the presence or not of edematous or fibrous component, infiltration and lymphoplasmocytic infiltrates.

Evaluation to cytokine concentration in serum for patients with nasal sinus polyposis1 day

The measurement to cytokine concentration in serum (mg/l)

Identify biological profiles for patients with nasal sinus polyposis1 day

The measurement to cytokine expression of naso-sinus polyps (RNA sequencing analysis)

Evaluation to quality of life by Sino-Nasal Outcome Test1 day

the measurement to quality of life by Sino-Nasal Outcome Test (test SNOT-22: test is a questionnaire that reviews 22 symptoms. Each item quantifies the severity of the symptom from 0 (no problem) to 5 (very severe problem). The maximum score is 110, a high score indicating a significant impact of symptoms).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Chu Poitiers

🇫🇷

Poitiers, France

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