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Clinical Trials in Canada / NCT03004326
Recruiting Observational

Clinical Transcriptomics in Systemic Vasculitis (CUTIS)

NCT03004326 · tracked via the Priya Life Science Canada tracker
Sponsor
Peter Merkel
Phase
Observational
Started
2017-01
Last updated
2026-01-22

Condition(s) studied

Cryoglobulinemic Vasculitis (CV)Drug-induced VasculitisEosinophilic Granulomatosis With Polyangiitis (EGPA)IgA VasculitisIsolated Cutaneous VasculitisGranulomatosis With Polyangiitis (GPA)Microscopic Polyangiitis (MPA)Polyarteritis Nodosa (PAN)Urticarial VasculitisVasculitis

Study summary

Multi-center observational study to evaluate the histopathology and transcriptome of cutaneous lesions in patients with several different types of vasculitis.

Eligibility

Sex
ALL
Min age
5 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Have a cutaneous lesion (purpuric macules, palpable purpura, retiform purpura, nodules, ulcers, or urticarial) believed to be related to active vasculitis * Have a suspected or confirmed diagnosis of: * 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 * Be willing and able to provide written informed consent (or assent for those under Exclusion Criteria: * You are less than five years old * Considered not to be a candidate for a biopsy or have a higher risk of developing an infection, bleeding, etc., from the biopsy, or a doctor believes that the risks for you participating in this study do not outweigh the potential benefit of learning information from your biopsy * You have a neutrophil count (type of white blood cell) less than 1500/mm3, platelet count less than 50,000/mm3, or a hemoglobin less than 7 g/dL * You have an uncontrolled disease that could prevent you from completing the study procedures * You have an active infection at or near the potential biopsy site, have poor circulation, or have bony prominence or other structure that would increase your risk of complications if you participated in this study * You are pregnant or nursing * You are not able to provide informed consent

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
University of California, Los Angeles Los Angeles California Completed
Boston University School of Medicine Boston Massachusetts Completed
Mayo Clinic Rochester Minnesota Completed
Cleveland Clinic Cleveland Ohio Completed
Oregon Health & Science University Portland Oregon Completed
University of Pennsylvania Philadelphia Pennsylvania Recruiting
University of Utah Salt Lake City Utah Completed
University of Virginia Charlottesville Virginia Recruiting
St. Joseph's Healthcare Hamilton Ontario Recruiting
University of Toronto Mount Sinai Hospital Toronto Ontario Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03004326 on ClinicalTrials.gov ↗ ← All trials in Canada