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BÜHLMANN BAT (Basophil Activation Test) in Allergy Diagnosis (Exploratory Pilot Study)

The goal of this exploratory pilot study is to generate early data needed for future validation studies of the automated BÜHLMANN BAT (Basophil activation test) assay. The main questions it aims to answer are: Does the BAT assay use the optimal allergen concentrations for stimulation, and how do its preliminary cut-off

Condition(s)Allergy Testing, Peanut Allergies, Venom Allergy, House Dust Mite Allergy, Hazelnut Allergy, Cat Epithelium Allergy
StatusRecruiting
Study typeObservational
SummaryThe goal of this exploratory pilot study is to generate early data needed for future validation studies of the automated BÜHLMANN BAT (Basophil activation test) assay. The main questions it aims to answer are: Does the BAT assay use the optimal allergen concentrations for stimulation, and how do its preliminary cut-offs perform in a real-world clinical scenario? Participants older than 1.5 years who are being evaluated for possible allergy sensitization will provide one additional blood tube during their routine blood draw as part of the regular medical care. The study involves only one visit and does not provide direct personal benefit.
Who can participateInclusion Criteria: * Individuals with diagnosis of a hypersensitivity / allergy to one of the 6 allergens, established according to common clinical practice Exclusion Criteria: * Pregnant women * Children under the age of 18 months * Individuals under therapy with Omalizumab or Rituximab * Individuals with an allergic reaction less than two weeks before blood sample collection * Individuals under therapy with BTK inhibitors * Individuals receiving allergen specific immunotherapy (ASIT) * Subjects with active infection and inflammatory conditions * Patients who are unable to understand the study information and informed consent form in German
Ages18 Months
SexAll
Lead sponsorBühlmann Laboratories AG
LocationsMünchen, Germany
Start date2026-05
NCT IDNCT07596303
Official listinghttps://clinicaltrials.gov/study/NCT07596303

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