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

Primary Purpose

Cystic Fibrosis, Rhinosinusitis, Lung Diseases

Status
Terminated
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Tobramycin nebulized nasally
Physiologic serum nebulized nasally
Sponsored by
Virginie ESCABASSE
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring cystic fibrosis, chronic rhinosinusitis, Lung Diseases, tobramycin, nebulized sonic aerosol therapy

Eligibility Criteria

7 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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 7 years or more because as they have a better adherence to nebulization treatment than younger children.
  • Diagnosis of cystic fibrosis confirmed by sweat test (>60mmol/L) and/or the identification of two CF-causing mutations
  • Confirmed chronic rhinosinusitis by Ear Nose and Throat doctor by endoscopic examination: bilateral mucopurulent secretions at middle meatus present longer than 12 weeks 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's parent for children)
  • Social security affiliation

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 between treatment 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's parent for children)

Sites / Locations

  • Centre Hospitalier Universitaire de Clermont ferrand
  • Centre Hospitalier Intercommunal de Créteil
  • Centre Hospitalier Universitaire de la Timone
  • Centre Hospitalier Universitaire De Nantes
  • Centre Hosiptalier de Nice
  • Centre Hospitalier Universitaire de Toulouse

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Tobramycin nebulized nasally

Physiologic serum nebulized nasally

Arm Description

Nebulized Tobramycin, one bulb (tobramycin 300 mg and sodium chloride 11.25 mg) nasally twice a day for 15 days

Nebulized sodium chloride 0.9%, one bulb twice a day nasally for 15 days

Outcomes

Primary Outcome Measures

Density of bacteria (in CFU/g log10) in sinus ostia of middle meatus samples at day 15

Secondary Outcome Measures

density of bacteria (in CFU/g log10) in sinus ostia of middle meatus samples at day 30 and 90
Minimum inhibitor concentration of sputum bacteria to antibiotics
Minimum inhibitor concentration of sputum bacteria to tobramycin
Force Vital capacity (FCV) in both groups
Forced Expiratory Volume in one second (FEV1) in both groups
nasal obstruction at day 90 compared to baseline
rhinorrhea compared to baseline
mucopurulent secretions compared to baseline
facial pain compared to baseline
dysosmia compared to baseline
Nasal endoscopic scores compared to baseline in both groups
Score of the SM5 quality of life questionnaire in both groups
Score of the SNOT20 quality of life questionnaire in both groups
Hearing perception of the intensity (in db) and tone (Hz) of sound waves

Full Information

First Posted
June 22, 2016
Last Updated
February 14, 2023
Sponsor
Virginie ESCABASSE
Collaborators
Henri Mondor University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02888730
Brief Title
Tobramycin Delivered by Nebulized Sonic Aerosol for Chronic Rhinosinusitis Treatment of Cystic Fibrosis Patients
Acronym
AVASMUC
Official Title
Efficacy of Antibiotic (Tobramycin) Delivered by Nebulized Sonic Aerosol for Chronic Rhinosinusitis Treatment of Cystic Fibrosis Patients: A Multicenter Double-blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Terminated
Why Stopped
No suffisant recruitment
Study Start Date
February 16, 2017 (Actual)
Primary Completion Date
May 16, 2017 (Actual)
Study Completion Date
July 8, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Virginie ESCABASSE
Collaborators
Henri Mondor University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Rhinosinusitis, Lung Diseases
Keywords
cystic fibrosis, chronic rhinosinusitis, Lung Diseases, tobramycin, nebulized sonic aerosol therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
86 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tobramycin nebulized nasally
Arm Type
Experimental
Arm Description
Nebulized Tobramycin, one bulb (tobramycin 300 mg and sodium chloride 11.25 mg) nasally twice a day for 15 days
Arm Title
Physiologic serum nebulized nasally
Arm Type
Placebo Comparator
Arm Description
Nebulized sodium chloride 0.9%, one bulb twice a day nasally for 15 days
Intervention Type
Drug
Intervention Name(s)
Tobramycin nebulized nasally
Other Intervention Name(s)
Tobramycin
Intervention Description
Two sonic nebulizations per day will be realized by patients: morning and evening during 15 days. There should be a maximum of 12 hours between the 2 doses but shall not be less than 6 hours. The dosage should not be adjusted to body weight. All patients will receive one ampoule of tobramycin twice a dayAmpoules of tobramycin are filled by 5 ml containing 300 mg of tobramycin and 11.25 mg of sodium chloride. Bulb should be employed in nebulizer and administered by the inhalation route approximately 15 minutes to complete.Antibiotic retained for the study, tobramycin is manufactured by the "Pharmacie à Usage Interne" of the Henri Mondor Hospital. The study's product will be prepared with Base Tobramycin and excipients in accordance with TOBI's composition.
Intervention Type
Drug
Intervention Name(s)
Physiologic serum nebulized nasally
Other Intervention Name(s)
sodium chloride 0.9%
Intervention Description
Two sonic nebulizations per day will be realized by patients: morning and evening during 15 days. There should be a maximum of 12 hours between the 2 doses but shall not be less than 6 hours. The dosage should not be adjusted to body weight. All patients will receive one ampoule of placebo (Nacl 0.9%) twice a day.Ampoules of placebo are filled by 5 ml containing of sodium chloride. Bulb should be employed in nebulizer and administered by the inhalation route approximately 15 minutes to complete. Placebo for the study is manufactured by the "Pharmacie à Usage Interne" of the Henri Mondor Hospital. Patients in placebo arm will receive 5ml of sodium chloride with the same color (light yellow transparent) as tobramycin
Primary Outcome Measure Information:
Title
Density of bacteria (in CFU/g log10) in sinus ostia of middle meatus samples at day 15
Time Frame
15 days
Secondary Outcome Measure Information:
Title
density of bacteria (in CFU/g log10) in sinus ostia of middle meatus samples at day 30 and 90
Time Frame
day 30 and day 90
Title
Minimum inhibitor concentration of sputum bacteria to antibiotics
Time Frame
day 15, 30 and 90
Title
Minimum inhibitor concentration of sputum bacteria to tobramycin
Time Frame
day 90
Title
Force Vital capacity (FCV) in both groups
Time Frame
day 0 and day 30
Title
Forced Expiratory Volume in one second (FEV1) in both groups
Time Frame
day 0 and day 30
Title
nasal obstruction at day 90 compared to baseline
Time Frame
day 0, 15, 30 and 90
Title
rhinorrhea compared to baseline
Time Frame
day 0, 15, 30 and 90
Title
mucopurulent secretions compared to baseline
Time Frame
day 0, 15, 30 and 90
Title
facial pain compared to baseline
Time Frame
day 0, 15, 30 and 90
Title
dysosmia compared to baseline
Time Frame
day 0, 15, 30 and 90
Title
Nasal endoscopic scores compared to baseline in both groups
Time Frame
day 0, 15, 30 and 90
Title
Score of the SM5 quality of life questionnaire in both groups
Time Frame
day 0, 15, 30 and 90
Title
Score of the SNOT20 quality of life questionnaire in both groups
Time Frame
day 0, 15, 30 and 90
Title
Hearing perception of the intensity (in db) and tone (Hz) of sound waves
Time Frame
day 0 and day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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 7 years or more because as they have a better adherence to nebulization treatment than younger children. Diagnosis of cystic fibrosis confirmed by sweat test (>60mmol/L) and/or the identification of two CF-causing mutations Confirmed chronic rhinosinusitis by Ear Nose and Throat doctor by endoscopic examination: bilateral mucopurulent secretions at middle meatus present longer than 12 weeks 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's parent for children) Social security affiliation 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 between treatment 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's parent for children)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginie Escabasse, MD
Organizational Affiliation
Creteil Hospital center (CHIC)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier Universitaire de Clermont ferrand
City
Clermont Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Centre Hospitalier Intercommunal de Créteil
City
Creteil
ZIP/Postal Code
94000
Country
France
Facility Name
Centre Hospitalier Universitaire de la Timone
City
Marseille
ZIP/Postal Code
13385
Country
France
Facility Name
Centre Hospitalier Universitaire De Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Centre Hosiptalier de Nice
City
Nice
ZIP/Postal Code
06002
Country
France
Facility Name
Centre Hospitalier Universitaire de Toulouse
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No
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Tobramycin Delivered by Nebulized Sonic Aerosol for Chronic Rhinosinusitis Treatment of Cystic Fibrosis Patients

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