The Journal of Allergy and Clinical Immunology
Volume 116, Issue 6 , Pages 1289-1295, December 2005

Treating acute rhinosinusitis: Comparing efficacy and safety of mometasone furoate nasal spray, amoxicillin, and placebo

  • Eli O. Meltzer, MD

      Affiliations

    • From the Allergy and Asthma Medical Group and Research Center, San Diego
    • Corresponding Author InformationReprint requests: Eli O. Meltzer, MD, Allergy and Asthma Medical Group and Research Center, 9610 Granite Ridge Drive, Suite B, San Diego, CA 92123.
  • ,
  • Claus Bachert, MD, PhD

      Affiliations

    • Ear, Nose and Throat Department, University Hospital Ghent, Ghent, Belgium
  • ,
  • Heribert Staudinger, MD

      Affiliations

    • Schering-Plough Research Institute, Kenilworth, NJ

Received 28 April 2005; received in revised form 21 July 2005; accepted 24 August 2005. published online 24 October 2005.

San Diego, Calif, Ghent, Belgium, and Kenilworth, NJ

Background

Intranasal corticosteroids used with antibiotics are known to improve rhinosinusitis symptoms compared with antibiotic therapy alone. However, the efficacy of intranasal corticosteroid monotherapy for acute, uncomplicated rhinosinusitis is not established.

Objectives

To evaluate efficacy and safety of mometasone furoate nasal spray (MFNS) versus amoxicillin and placebo in patients with acute, uncomplicated rhinosinusitis.

Methods

In this double-blind, double-dummy trial, subjects (≥12 years; N = 981) were randomized to MFNS 200 μg once daily or twice daily for 15 days, amoxicillin 500 mg 3 times daily for 10 days, or respective placebo. Follow-up was 14 days. The primary efficacy endpoint was mean am/pm major symptom score over the treatment phase. Secondary efficacy endpoints included total symptom score. Safety assessments included disease recurrence during follow-up and adverse event monitoring.

Results

Mometasone furoate nasal spray 200 μg twice daily was significantly superior to placebo (P < .001) and amoxicillin (P = .002) at improving major symptom score. Starting on day 2, MFNS 200 μg twice daily improved total symptom score throughout treatment versus amoxicillin (P = .012) and placebo (P < .001). Global response to treatment was significantly greater with MFNS 200 μg twice daily versus amoxicillin (P = .013) and placebo (P = .001). Although significantly superior to placebo, MFNS 200 μg once daily was not superior to amoxicillin for the primary or secondary efficacy endpoints. All treatments were well tolerated with a similar incidence of adverse events.

Conclusion

In patients with acute, uncomplicated rhinosinusitis, MFNS 200 μg twice daily produced significant symptom improvements versus amoxicillin and placebo, without predisposing the patient to disease recurrence or bacterial infection.

Key words: Acute rhinosinusitis, amoxicillin, intranasal corticosteroid, mometasone furoate, symptoms

Abbreviations used: MFNS, Mometasone furoate nasal spray, MSS, Major symptom score, TSS, Total symptom score

 

 Disclosure of potential conflict of interest: E. Meltzer received grant support from Schering-Plough for this study and is a consultant on the speakers' bureau and has received grants from numerous pharmaceutical companies. H. Staudinger and C. Bachert have disclosed no conflict of interest.Supported by a grant from the Schering-Plough Research Institute.

PII: S0091-6749(05)01934-2

doi:10.1016/j.jaci.2005.08.044

The Journal of Allergy and Clinical Immunology
Volume 116, Issue 6 , Pages 1289-1295, December 2005