The purpose of this study is to compare Rhinocort with placebo in pediatric subjects aged 2-5 years with allergic rhinitis to study effects on nasal symptoms such as sneezing, runny and stuffy noses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
650
To compare Rhinocort with placebo to compare effects on nasal symptoms such as sneezing, runny and stuffy noses as assessed by caregivers.
Time frame: At 2 weeks
Safety assessment via adverse events and clinical measurements
Time frame: At 1 & 2 weeks
To assess efficacy of Rhinocort via the physician and caregivers assessments
Time frame: At 2 weeks
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