Allergic Rhinoconjunctivitis Clinical Trial
Official title:
A Randomized, Double-blinded, Parallel-group, Placebo-controlled Clinical Study of the Efficacy and Safety of an Oral Nutraceutical (Lertal®) as an add-on to Standard Therapy for Allergic Rhinoconjunctivitis in Pediatrics
The purpose of this study is to evaluate the efficacy and safety of Lertal® as an add-on treatment for children affected by allergic rhinoconjunctivitis.
Allergic rhinoconjunctivitis (AR) is a common chronic disorder in children, especially in
developed countries. It is not characterized by nasal symptoms only (such as congestion and
sneezing), but may also cause general complaints such as fatigue and cough. AR can also have
detrimental effects on mood, sleep, social activities and scholastic performance.
Lertal® is a novel nutraceutical containing seed extracts from Perilla Frutescens, Quercetin
extracted from Sophora japonica and Vitamin D3, all compounds that have demonstrated their
ability to reduce allergy symptoms and the use of anti-allergy drugs in adults.
The aim of this randomized, double-blinded, parallel-group, placebo-controlled study is to
evaluate the efficacy and safety of Lertal® as an add-on treatment for children affected by
allergic rhinoconjunctivitis.
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