About this trial
The purpose of this study is to collect clinical, laboratory, and instrumental data from patients with eosinophilic granulomatosis with polyangiitis or hypereosinophilic syndrome, which will then be analyzed using artificial intelligence techniques with the aim of identifying characteristics that differentiate the two diseases and can predict the response to the treatment plan.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 years of age or over
A diagnosis of EGPA or HES
Willing and able to give informed written consent, or willing to give permission for a nominated friend or relative to provide written informed assent if they are unable to do so because of physical disabilities
Disqualifiers
Lack of a confirmed diagnosis of EGPA or HES.
Other causes of eosinophilia
Trial design
Parallel
Treatments tested in this trial
Blood draw for the laboratory assessment
Procedure/SurgeryBlood draw for the laboratory assessment
Treatment groups
Trial outcomes
Primary outcomes
characteristics that are different between HES and EGPA
Sponsors and contacts
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