The objective of this study is to evaluate the efficacy and safety of specific subcutaneous immunotherapy with modified allergen extracts.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
subcutaneous injections
subcutaneous injections
Unnamed facility
Madrid, Spain
Symptom and medication score
Time frame: 1 year
Safety of the treatment
Time frame: 1 year
Documentation of adverse events
Time frame: 1 year
Clinical global improvement
Time frame: 1 year
Quality of Life Questionnaire
Time frame: 1 year
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