Tobramycin Delivered by Nebulized Sonic Aerosol for Chronic Rhinosinusitis Treatment of Cystic Fibrosis Patients

Last updated: February 14, 2023
Sponsor: Virginie ESCABASSE
Overall Status: Terminated

Phase

3

Condition

Cystic Fibrosis

Soft Tissue Infections

Scar Tissue

Treatment

N/A

Clinical Study ID

NCT02888730
AVASMUC
  • Ages > 7
  • All Genders

Study Summary

Patients with cystic fibrosis frequently develop chronic rhinosinusitis. Bacterial colonization is facilitated by a reduced mucociliary function and some previous studies suggest that the microbiology of the upper airways might influence the microbiology of the lower airway. The aim of this randomized control study is to demonstrate efficacy of antibiotic delivered by nebulized sonic aerosol therapy to decrease the bacterial load in sinuses and medium ostia and to improve the sino-nasal symptoms and endoscopic scores, quality of life and lung function

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients older than 7 years followed in the 6 CRCM centers (Créteil, Marseille,Nantes, Toulouse, Clermont-Ferrand and Nice). We choose to enroll children aged 7years or more because as they have a better adherence to nebulization treatment thanyounger children.
  • Diagnosis of cystic fibrosis confirmed by sweat test (>60mmol/L) and/or theidentification of two CF-causing mutations
  • Confirmed chronic rhinosinusitis by Ear Nose and Throat doctor by endoscopicexamination: bilateral mucopurulent secretions at middle meatus present longer than 12weeks with or without nasal polyps
  • Positive bacteria susceptibility to tobramycin in samples from middle meatus
  • Susceptibility of bacteria to tobramycin confirmed
  • Pulmonary examination before enrollment
  • Written informed consent obtained at enrollment for all patients (consent of minor'sparent for children)
  • Social security affiliation

Exclusion

Exclusion Criteria:

    • Oral antibiotic therapy one month before enrollment
  • enrollment in another protocol with antibiotic
  • Ongoing aerosolized tobramycin for endobronchial infection to avoid an overlap betweentreatment for lung and treatment for sinusitis
  • Abnormal auditory acuity (decrease of 20dB in auditory acuity)
  • Hypersensibility or allergenecity of aminoglycosides
  • FEV < 25% or FVC of 40% or more of the value predicted for height
  • Transplant patient or patient on transplant list
  • Patient under nasal oxygen or under noninvasive ventilation
  • Pregnant woman
  • Breast-feeding
  • No Social security affiliation
  • Informed consent non obtained at enrollment for all patients (consent of minor'sparent for children)

Study Design

Total Participants: 86
Study Start date:
February 16, 2017
Estimated Completion Date:
July 08, 2019

Study Description

Cystic fibrosis (CF) is the most common lethal autosomal recessive disorder in the Caucasian population affecting ~1:3000 children, with a carrier frequency of 1:25. It is a multisystem disorder where pulmonary and sinonasal involvements occur in 90-100% of patients, and up to 86% of children have nasal polyps . Patients with CF develop chronic rhinosinusitis (CRS) due to the defect in the cystic fibrosis Transmembrane Regulator (CFTR) protein. The membrane lining the paranasal sinuses and the nose is identical to the membrane lining the lungs. As in lower airways (LAW) the defect CFTR protein result in viscous mucus . Consequently mucociliary function is reduced, which facilitates bacterial colonization and eventually infection leading to rhinosinusitis . In the past decades infection of the lower airways was the most prominent focus in treatment protocols for CF. Over the years infection of the upper airways (UAW) gradually gained more attention in CF.

Previous research in the microbiology of the upper airways (UAW) in CF displayed that Haemophilus influenzae, Pseudomonas aeruginosa and Staphylococcus aureus were most frequently cultures from the UAW . Since several studies showed concordance between organisms in the UAW and the LAW in CF, the hypothesis evolved that the UAW might influence the patient pulmonary status . Moreover, comparison of UAW and and LAW cultures in CF adult patients showed that Pseudomonas aeruginosa can be cultured from the UAW after eradication therapy which may suggest persistence of Pseudomonas aeruginosa in the UAW . This problem is highlighted in double lung transplant where UAW also appears as a protective niche of adapted clones of bacteria, which can intermittently spread this pathogen to the lung.

CRS treatment in CF patients is based on daily nasal lavages but above all on local or systemic antibiotic treatments to eradicate bacteria in sinuses . Local therapy is favoured in CRS treatment of CF patients to avoid antibiotic side effects, changing organisms or resistance patterns. Sonic aerosol therapy with antibiotics for 15 days is commonly used for CRS in non CF patients to improve sinonasal symptoms and reduce purulent secretions as sound addition in pneumatic aerosol in head corpse's models creates an acoustic pressure at the ostia to improve the aerosol penetration in maxillary sinuses . However its efficacy on bacterial carrying in sinuses is not proved . At the opposite, efficacy of aerosol of tobramycin to LAW was proved in CF patients with a decrease of the density of Pseudomonas aeruginosa, an improvement of FEV, and fewer pulmonary exacerbations .

At the present time, efficacy of antibiotic (tobramycin) delivered by nebulized sonic aerosol for CRS treatment of CF patients is unknown particularly on bacterial carrying.

The aim of this study is to demonstrate that nebulized sonic aerosol therapy with tobramycin in Cystic Fibrosis patients decreases significantly bacterial carrying in sinuses, sinus ostia of middle meatus and sputum compared to nebulized sonic aerosol therapy with placebo and that nebulized sonic aerosol therapy improves sino-nasal symptoms and endoscopic scores, quality of life and lung function.

Connect with a study center

  • Centre Hospitalier Universitaire de Clermont ferrand

    Clermont Ferrand, 63003
    France

    Site Not Available

  • Centre Hospitalier Intercommunal de Créteil

    Creteil, 94000
    France

    Site Not Available

  • Centre Hospitalier Universitaire de la Timone

    Marseille, 13385
    France

    Site Not Available

  • Centre Hospitalier Universitaire De Nantes

    Nantes, 44093
    France

    Site Not Available

  • Centre Hosiptalier de Nice

    Nice, 06002
    France

    Site Not Available

  • Centre Hospitalier Universitaire de Toulouse

    Toulouse, 31059
    France

    Site Not Available

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