Clinical Transcriptomics in Systemic Vasculitis (CUTIS)
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- STATUS
- Recruiting
Summary
This study employs a multi-center approach to evaluate cutaneous vasculitis across several forms of idiopathic vasculitis. Patients with cutaneous manifestations of vasculitis will be evaluated by teams of primary vasculitis care providers and Dermatologists in order to facilitate optimal selection of patients and sampling of lesions. A punch skin biopsy at a site of active vasculitis will be the source of material for histopathologic and transcriptomic evaluation. The histopathology of cutaneous vasculitis will be characterized using a standardized, systematic approach. This approach includes a detailed description of abnormalities and extensive immunophenotyping of cell populations in the epidermal, dermal, and subcutaneous layers of skin. In addition to histologic description, skin biopsy material will be used a source of RNA for whole-genome gene expression profiling studies. Differential gene expression comparisons will be made across types of vasculitis. Disease-agnostic computational approaches will be used to discover novel ways to classify subgroups based upon global and specific patterns of gene expression. Additional samples will be collected (whole blood RNA, DNA) for potential secondary studies.
Details
Condition | ['Cryoglobulinemic Vasculitis (CV)', 'Drug-induced Vasculitis', 'Eosinophilic Granulomatosis With Polyangiitis (EGPA)', 'IgA Vasculitis', 'Isolated Cutaneous Vasculitis', 'Granulomatosis With Polyangiitis (GPA)', 'Microscopic Polyangiitis (MPA)', 'Polyarteritis Nodosa (PAN)', 'Urticarial Vasculitis', 'Vasculitis'] |
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Age | 99years or below |
Clinical Study Identifier | TBD |
Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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