Asthma Clinical Trial
Official title:
Safety and Efficacy of Ultra-Rush High-Dose Sublingual Immunotherapy in Children With Asthma Allergic to Grass Pollen - Prospective, Randomized, Placebo Controlled Study.
The aim of the study is to assess the safety and efficacy of sublingual immunotherapy applied preseasonal and seasonal in ultra-rush scheme in children with bronchial asthma allergic to grass pollen. The investigators will assess clinical symptoms, reliever drugs usage, lung function, chosen markers of allergic inflammation, bronchial hyperreactivity with methacholine, and presence and type of allergy after two years of sublingual immunotherapy (SLIT) in children with asthma.
Specific immunotherapy is the only causal treatment method of atopic diseases including
bronchial asthma in children. Sublingual immunotherapy seems to be the most promising
alternative to traditional specific subcutaneous injection immunotherapy.
The aim of the study is to assess the safety and efficacy of sublingual immunotherapy
applied preseasonal and seasonal in ultra-rush scheme in children with bronchial asthma
allergic to grass pollen. We will assess clinical symptoms, reliever drugs usage, lung
function, chosen markers of allergic inflammation, bronchial hyperreactivity with
methacholine, and presence and type of allergy after two years of SLIT in children with
asthma.
After two years the study will be unblinded, all the children will be given grass pollen
allergen extract for a year.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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