Patient Library for Pruritus Sine Materia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort will collect blood, a skin biopsy, a skin swab, and five patient questionnaires at enrollment, then repeat the same questionnaires and clinical data annually for five years. No further biological samples are planned after baseline. The aim is to link clinical features with biological data to improve knowledge about pruritus sine materia etiologies. The study is conducted at the dermatology service of CHRU Brest with University Hospital, Brest as the lead sponsor.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Diagnosis of pruritus sine materia
* Collection of consent
* Adult

Exclusion Criteria:

\- Refusal to participate in the study

Where it's running

• Service de dermatologie, CHRU BREST
  Brest, France Recruiting

Study contacts

• Study coordinator: Laurent MISERY
• Email: laurent.misery@chu-brest.fr
• Phone: 02 98 22 33 15

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.