The objective of this study is to assess the efficacy and safety of cluster immunotherapy with highly polymerized allergen extracts.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
121
cluster schedule
cluster schedule
Zentrum für Rhinologie und Allergologie
Wiesbaden, Germany
Symptom and medication score
Time frame: 1 year
Safety of the treatment during the study period
Time frame: 1 year
Documentation of adverse events
Time frame: 1 year
Individual symptom scores of the rhinoconjunctivitis symptom score (RSS) during the pollen season
Time frame: 1 year
Global evaluation and Quality of life questionnaire
Time frame: 1 year
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