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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Mucocutaneous symptoms from NSAIDs | Active Comparator |
| |
| Respiratory symptoms from NSAIDs | Active Comparator |
| |
| NSAIDs tolerant individuals | Active Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Lysine-ASA Nasal ProvocationTest | Procedure | Lysine-ASA 80 µl (16 mg of aspirin) will be installed in both nostrils with pipette |
|
| Measure | Description | Time Frame |
|---|---|---|
| Symptom scores and/or acoustic rhinometry result upon Lysine-ASA nasal provocation test in patients with history of mucocutaneous or respiratory symptoms from NSAIDs | 5 months |
| Measure | Description | Time Frame |
|---|---|---|
| Correlation between clinical manifestations and laboratory results (basophil activation test, etc.) | 5 months |
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Inclusion Criteria:
Exclusion Criteria:
Patients who cannot discontinue drugs before the test as follow
Contraindicated for nasal provocation test: pregnant, exacerbation of allergic rhinitis/asthma, having upper respiratory tract infection within 2 weeks prior to the test, having nose surgery within 8 weeks prior to the test, having severe systemic disease(s)
Having factors interfere nasal provocation test with Lysine-ASA such as massive nasal polyp, nasal septal perforation, total nasal obstruction at least 1 nostril
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| Name | Affiliation | Role |
|---|---|---|
| Jettanong Klaewsongkram, MD | Chulalongkorn University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Faculty of Medicine, Chulalongkorn University | Bangkok | 10330 | Thailand |
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