Evaluation of the Efficacy of Azithromycin in Idiopathic Purulent Oedematous Sinusitis in Adults (SOPAZITHRO)

Evaluation of the Efficacy of 3-month Continuous Extended Treatment With Azithromycin in Idiopathic Purulent Oedematous Sinusitis in Adults: a Multicentre Randomised Controlled Trial

Purulent Oedematous Sinusitis (POS) is a particular form of chronic rhinosinusitis observed in 2% of the general population. In spite of its heavy impact on the quality of life, There is no established recommendation for the treatment of primary POS. Long-term low-dose macrolides are currently proposed for these forms of chronic rhinosinusitis when conventional treatments (local corticosteroids, saline rinsing, iterative short courses of antibiotics targeted on pathogens, and surgical opening and drainage) have failed. This treatment with macrolides is currently applied off-label.

This study aims to assess the efficacy of macrolides in POS. An extensive workup is fulfilled to exclude other forms of chronic rhinosinusitis (Th2 biased inflammatory diseases, allergic diseases) (allergy, nasosinusal polyposis) or those due to cystic fibrosis or immune deficiency.

Study Overview

• Status: Recruiting
• Conditions: Sinusitis, Chronic; Sinus Infection Chronic
• Intervention / Treatment: Drug: Azithromycin Oral Tablet; Drug: Placebo

Detailed Description

POS is a particular form of chronic rhinosinusitis described in 2% of the general population. They lead to an alteration in the quality of daily life with a significant impact on the professional life of 70% of patients. They can be of idiopathic or of secondary origin. The most frequent secondary forms are those observed in cystic fibrosis and immune deficiencies. The pathophysiology of primary POS remains poorly understood, involving Th1-type inflammation and various bacteria (with Staphylococcus Aureus in the forefront). Bacteria could impair the ciliary beat, perpetuating infection and mucosal inflammation. There is no established recommendation for the treatment of primary POS Long-term low-dose macrolides are currently proposed for these forms of chronic rhinosinusitis when conventional treatments (local corticosteroids, saline rinsing, iterative short courses of antibiotics adapted to the germs found, and surgical drainage) have failed. This treatment with macrolides is currently used off label.

Macrolides are effective on most gram-positive and gram-positive bacteria. Macrolides also have immunomodulatory properties on the Th1 immune response. This effect is maintained even in the presence of macrolide-resistant bacteria. In chronic obstructive pulmonary disease, daily administration of half-dose macrolides over the long term (HDLT) has been shown to be effective in reducing the frequency of infectious exacerbations. Uncontrolled trials have described an improvement in symptom scores in chronic rhinosinusitis with or without polyps. The results observed in randomized trials versus placebo are contradictory. A meta-analysis published in 2013 based on these 2 randomized studies was inconclusive regarding the efficacy of HDLT macrolides. The heterogeneity of the inclusion criteria with rhinosinusitis of a different proTh-2 inflammatory profile corresponding to that usually observed in nasal polyposis could explain this lack of result. A review of the literature published in 2017 on HDLT macrolides based on 52 publications observed a very wide diversity of antibiotic protocols in terms of the molecule chosen, the administration scheme and the duration of treatment (8 to 24 weeks). The number of patients studied was often small, which affected the statistical power of the results obtained. The authors of this review conclude by stressing the need to conduct placebo-controlled studies on large populations of patients selected on the phenotypic level.

This study propose to evaluate the value of HDLT macrolides in this specific etiological setting. This project plans to exclude all chronic rhinosinusitis of Th2 inflammatory origin (allergy, nasosinusal polyposis) or those due to cystic fibrosis or immune deficiency. In addition, the inclusion centers selected in Ile de France have the necessary expertise to evaluate the impact of azithromycin on mucociliary clearance, notably with the development of innovative tools to measure the efficiency of the ciliary beat (high-speed video microscopy and particle tracking).At the same time, the tolerance of HDLT macrolides measured in patients with cystic fibrosis or chronic obstructive pulmonary disease (COPD) is excellent, provided that the well-documented contraindications are respected. No serious adverse effects have been reported, apart from cases of transient or permanent moderate hearing loss requiring audiometric monitoring.

No specific study regarding the treatment of primary POS is available to date, even tough POS is very prevalent and its management is still associated with poor patient-reported outcomes.

• Study Type: Interventional
• Enrollment (Estimated): 230
• Phase: Phase 3

Contacts and Locations

• Study Contact: Name: Emilie BEQUIGNON; Phone Number: +33 0145175000; Email: emilie.bequignon@chicreteil.fr
• Study Contact Backup: Name: Camille JUNG; Phone Number: +33 0145175000; Email: camille.jung@chicreteil.fr

Study Locations

• France
  • Créteil, France, 94010
    • Not yet recruiting
    • Hopital Henri Mondor
    • Contact: Sophie BARTIER
  • Le Kremlin-Bicêtre, France
    • Not yet recruiting
    • CHU Bicêtre, AP-HP
    • Contact: Jean-François PAPON
  • Lille, France, 59000
    • Recruiting
    • CHU Lille
    • Contact: Geoffrey MORTUAIRE; Email: Geoffrey.MORTUAIRE@CHRU-LILLE.FR
  • Lyon, France
    • Not yet recruiting
    • CHU de la Croix Rousse
    • Contact: Clémentine Daveau
  • Lyon, France
    • Not yet recruiting
    • Hospices de Lyon
    • Contact: Maxime Fieux
  • Marseille, France, 13005
    • Not yet recruiting
    • Hôpitaux Universitaires de Marseille Conception
    • Contact: Justin MICHEL
  • Nancy, France
    • Recruiting
    • CHRU de Nancy
    • Contact: Cécile Rumeau
  • Nantes, France, 44093
    • Recruiting
    • Centre Hospitalier Universitaire de Nantes
    • Contact: Olivier Malard, MD PhD; Email: olivier.malard@chu-nantes.fr
  • Paris, France, 75010
    • Recruiting
    • Hopital Lariboisiere
    • Contact: Benjamin Verillaud
  • Toulouse, France
    • Recruiting
    • CHU Toulouse
    • Contact: Guillaume De Bonnecaze, MD
  • Ile De France
    • Créteil, Ile De France, France, 94000
      • Recruiting
      • Centre Hospitalier Intercommunal
      • Contact: André COSTE

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years to 68 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Patient older than 18 years and less than 70 years of age

• Chronic rhinosinusitis (> 12 weeks of evolution) meeting the definition published in the European Paper Position2012 (1) and corresponding exclusively to the following endoscopic and CT criteria:

  • Nasal endoscopy showing bilateral and diffuse involvement associating edema of the mucosa of the nasal cavities and meatus with the presence of mucopurulent secretions in these areas
  • Nasosinus CT scan showing diffuse and bilateral pansinus opacities involving at least the maxillary sinuses and the anterior and posterior ethmoids
• Persistent intractable purulent rhinosinusitis despite at least 2 antibiotic therapies
• Signed informed consent of the patient
• Membership in a health insurance plan or beneficiary

Exclusion Criteria:

• Pregnancy or breastfeeding
• PCOS of identified primary cause (identified immune deficiency, cystic fibrosis)
• Chronic non-purulent rhinosinusitis (nasosinusal polyposis, allergic rhinosinusitis)
• Localized chronic suppurative rhinosinusitis (single sinus, unilateral, frontal or maxillary or sphenoidal)
• Severe hepatic insufficiency (factor V level < 50%)
• Severe renal insufficiency (stage 4 (GFR < 30 ml/min/1.73 m2) and/or creatinine < 40 ml/min)
• Severe heart failure (old age, ischemic heart disease, episode of recurrent cardiac arrest; hypotension, NYHA functional stage III-IV; widened QRS, complex ventricular arrhythmias; hyponatremia (Na <135mmol/l); stage 4 renal failure (GFR < 30 ml/min/1.73 m2); severely depressed LVEF (< 30%)
• Documented moderate pre-existing hearing loss (>30dB) or single ear (unilateral cophosis)
• Major cognitive impairment or lack of French language skills preventing completion of SNOT-22 and SF-36 questionnaires
• Patient with galactose intolerance, total lactase deficiency or glucose-galactose malabsorption syndrome (rare hereditary diseases)
• Patient with peanut or soy allergy
• Patient allergic to macrolides
• Patients who are intolerant or allergic to any of the excipients of azithromycin or placebo
• Treatment with azithromycin in the previous 3 months
• Long QT on ECG ((>440ms for male and >450ms for female) or cardiac arrhythmia or bradycardia (<60btm)
• Hypokalemia or hypomagnesemia on blood ionogram
• Confirmed or suspected atypical mycobacteriosis
• Contraindicated drug combinations with macrolides (K-vitamins or drugs containing cisapride, colchicine, ergotamine or dihydroergotamine)

• Cautionary drug combinations (non-inclusion criteria)

  • Atorvastatin (Increased risk of concentration-dependent rhabdomyolysis-type adverse events due to decreased hepatic metabolism of the cholesterol-lowering drug.
  • Ciclosporin (risk of increased ciclosporin blood levels and creatinine levels)
  • Digoxin (increase in digoxemia due to increased absorption of digoxin), Drugs likely to cause torsades de pointes, in particular class IA (e.g. quinidine) and class III (e.g. amiodarone, sotalol) antiarrhythmics, antipsychotics (e.g. phenothiazines, pimozide), tricyclic antidepressants (e.g. citalopram), certain fluoroquinolones (e.g. moxifloxacin, levofloxacin) (increased risk of ventricular rhythm disturbances)
  • Simvastatin (increased risk of rhabdomyolysis-type adverse effects (concentration-dependent), due to decreased hepatic metabolism of the cholesterol-lowering agent)
  • Ivabradine (increased risk of ventricular rhythm disorders),
  • Hypokalemic drugs
  • Bradycardia drugs
• Patients with severe cholestasis
• Patients under guardianship or curatorship
• Patients with hematologic malignancies who have undergone hematopoietic stem cell transplantation
• History of facial radiotherapy
• History of rhinosinus cancer
• Participation in other category 1 research at the time of inclusion or in the month prior to inclusion

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Azithromycin oral tablet; Azithromycin 250 mg once daily morning or evening (with or without meals)	Drug: Azithromycin Oral Tablet; Treatment assigned by randomization will be prescribed immediately. The active or placebo will be dispensed by the centre's pharmacy. Treatment will be taken in the morning or evening for 3 months.; Other Names: active arm
Placebo Comparator: Placebo; Placebo once daily morning or evening (with or without meals)	Drug: Placebo; Treatment assigned by randomization will be prescribed immediately. The active or placebo will be dispensed by the centre's pharmacy. Treatment will be taken in the morning or evening for 3 months.; Other Names: comparator arm

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Comparison of sinonasal outcome test (SNOT) 22	Comparison of the means of the Sinonasal Outcome Test (SNOT 22) specific quality of life scores after 3 months of treatment. (min = 0, max = 110)	3 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of infectious rhinosinus exacerbations	The number of infectious rhinosinus exacerbations during the 3-month period,	3 months
Number of courses of antibiotics used	Number of courses of antibiotics used during the 3-month period other than azithromycin or placebo	3 months
Visual analog scales of symptoms	Visual analog scales (VAS) of symptoms (self-assessment) (nasal obstruction, rhinorrhea, facial pain, smell disorder, nasal hyperactivity, epistaxis). The VAS measures the intensity of pain on a scale from 0 to 10.	6 months
Semi-quantitative symptom scale	Semi-quantitative 4-point symptom scale assessed by the practitioner (min = 0, max = 3)	6 months
Semi-quantitative nasal endoscopy score	Semi-quantitative nasal endoscopy score (0: absent/1: present) for each of the following items: presence of pus, edema, erythema, crusts, polyps, scored out of 5 per nasal cavity (maximum score of 10) (Lund Kennedy score),	6 months
Quantitative Lund MacKay CT score	Quantitative Lund MacKay CT score (0: no sinus opacity, 1: moderate opacity, 2: total opacity) measured on 12 for each side (score of 24 maximum),	6 months
Nasal inflammation flow	Nasal inflammation (nasal nitric oxide (NO) flow, neutrophil polynuclear cell (NPC) and lymphocyte infiltrate on nasal cytology and assays of interleukin 6, 8 and elastase produced by NPCs in nasal secretions)	6 months
General quality of life	General quality of life Short form 36 (SF-36) (min=1, max=100)	6 months
Days off work	Number of days off work in the 3 months prior to treatment and the number of days off work during the 3 months of treatment	6 months
Olfactory score	Olfactory score (sniffing's stick test),	6 months
Bacteria present on the protected nasal swab	Identification and quantification of bacteria observed on the protected nasal swab (semi-quantitative score	6 months
Number of participants with clinical adverse events as assessed by compliance	Clinical tolerance evaluated by the effective intake of tablets	3 months
Number of participants with biological adverse events as assessed by compliance	Biological tolerance evaluated by the effective intake of tablets	3 months
Residual effect of the treatment using the SNOT 22 quality of life questionnaires	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the SNOT 22 quality of life questionnaires	6 months
Residual effect of the treatment using the SF-36 quality of life questionnaires	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the SF-36 quality of life questionnaires	6 months
Residual effect of the treatment using the VAS score	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the VAS score. The VAS measures the intensity of pain on a scale from 0 to 10.	6 months
Residual effect of the treatment using the semi-quantitative symptom scale	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the semi-quantitative symptom scale	6 months
Residual effect of the treatment using the nasal endoscopy	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the nasal endoscopy	6 months
Residual effect of the treatment using the bacteriological samples.	At 6 months (i.e., 3 months after cessation of treatment), the residual effect of treatment will be measured using the bacteriological samples.	6 months
Quantitative aspect of the ciliary beat	Quantitative aspect of the ciliary beat (frequency of the beat in Hertz) on a small number of centers having the equipment	6 months
Qualitative aspect of the ciliary beat	Qualitative aspect of the ciliary beat (coordination (normal or dyskinetic), index of efficiency)) on a small number of centers having the equipment	6 months

Collaborators and Investigators

• Sponsor: Centre Hospitalier Intercommunal Creteil

Study record dates

Study Major Dates

• Study Start (Actual): November 28, 2022
• Primary Completion (Estimated): March 1, 2025
• Study Completion (Estimated): June 1, 2025

Study Registration Dates

• First Submitted: October 28, 2021
• First Submitted That Met QC Criteria: December 1, 2021
• First Posted (Actual): December 15, 2021

Study Record Updates

• Last Update Posted (Actual): April 12, 2024
• Last Update Submitted That Met QC Criteria: April 11, 2024
• Last Verified: March 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Infections; Respiratory Tract Infections; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Paranasal Sinus Diseases; Nose Diseases; Sinusitis; Anti-Infective Agents; Anti-Bacterial Agents; Azithromycin
• Other Study ID Numbers: SOPAZITHRO; 2020-001227-13 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No