Perennial Allergic Rhinitis Clinical Trial
Official title:
A Randomized Two Period Two-Way Crossover Study To Evaluate Patient Preference, Satisfaction And Efficacy Of A Nasal Aerosol Versus An Aqueous Nasal Spray Used For The Treatment Of Allergic Rhinitis
This is a randomized, multicenter, 2-way crossover study in subjects 12 years or older with perennial allergic rhinitis (PAR) to evaluate patient preference, satisfaction and efficacy of ciclesonide nasal aerosol versus mometasone aqueous nasal spray. A novel patient-administered assessment, developed and validated to measure patient satisfaction with and preference of intranasal corticosteroids (INCS) for the treatment of allergic rhinitis (AR), is utilized in this study.
This is a randomized, multicenter, 2-way crossover study in subjects 12 years or older with
perennial allergic rhinitis (PAR) to evaluate patient preference, satisfaction and efficacy
of ciclesonide nasal aerosol versus mometasone aqueous nasal spray. A novel
patient-administered assessment, developed and validated to measure patient satisfaction
with and preference of intranasal corticosteroids (INCS) for the treatment of allergic
rhinitis (AR), is utilized in this study.
Subjects will be randomized to 1 of 2 treatment sequences:
Sequence 1: Treatment Period 1 = ciclesonide nasal aerosol 74 mcg once daily for two weeks;
Treatment Period 2 = mometasone nasal inhalation 200 mcg once daily for two weeks Sequence
2: Treatment Period 1 = mometasone nasal inhalation 200 mcg once daily for two weeks;
Treatment Period 2 = ciclesonide Nasal aerosol 74 mcg once daily for two weeks
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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