The objective of this clinical trial is to assess the safety and efficacy of sublingual application of allergen extracts for specific immunotherapy in patients suffering from perennial allergic rhinitis due to house dust mites.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
130
sublingual application
sublingual application
Unnamed facility
Madrid, Spain
Symptom and medication score
Time frame: 1 year
Safety of sublingual application
Time frame: 1 year
Protocol of adverse events
Time frame: 1 year
Quality of Life Questionnaire
Time frame: 1 year
Evaluation of patients' related clinical global improvement
Time frame: 1 year
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