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Clinical Trial Summary

Very little is currently known about the pathophysiology of pruritus sine materia according to the etiology. The creation of this cohort should make it possible to improve our clinical and biological knowledge according to the etiology, by collecting blood, skin, feces, and clinical data.


Clinical Trial Description

At inclusion, 52.5 ml of blood will be collected, then an additional skin biopsy and a skin swab. Five questionnaires will be filled in by the patient. At 6 months, then every years for 5 years, the same 5 questionnaires will be collected as well as the clinical data. However, no more biological samples will be collected. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05678309
Study type Observational [Patient Registry]
Source University Hospital, Brest
Contact Laurent MISERY
Phone 02 98 22 33 15
Email laurent.misery@chu-brest.fr
Status Not yet recruiting
Phase
Start date April 1, 2023
Completion date February 1, 2033

See also
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