This study aims to compare the efficacy of nasal provocation test with Lysine-Acetylsalicylate in patients with history of NSAIDs hypersensitivity between mucocutaneous symptoms and respiratory symptoms and laboratory outcomes.
Study Type
INTERVENTIONAL
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
34
Lysine-ASA 80 µl (16 mg of aspirin) will be installed in both nostrils with pipette
Faculty of Medicine, Chulalongkorn University
Bangkok, Thailand
Symptom scores and/or acoustic rhinometry result upon Lysine-ASA nasal provocation test in patients with history of mucocutaneous or respiratory symptoms from NSAIDs
Time frame: 5 months
Correlation between clinical manifestations and laboratory results (basophil activation test, etc.)
Time frame: 5 months
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