The aim of the study is to evaluate the prevalence of positive anti BP180 and/or anti BP230 serology in the serum of patients with chronic and diffuse pruritus for at least 1 month under immunotherapy and in the absence of obvious pruritic dermatosis (e.g. scabies, contact eczema...).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
100
For patients with positive anti BP180 and/or anti BP230 serology, a characterisation of the immunoglobulin subclasses will be performed
UHRouen
Rouen, France
RECRUITINGNumber of patients on immunotherapy with chronic diffuse pruritus for at least 1 month with positive anti BP180 and/or anti BP230 serology
Time frame: 1 day
Number of anti-BP180 and/or anti-BP230 positive patients who will develop urticarial, eczematous or bullous disease
Time frame: 30 days
Number of anti-BP180 and/or anti-BP230 positive patients who will develop urticarial, eczematous or bullous disease
Time frame: 1 year
Patient survival
Time frame: 1 year
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