Clinical Transcriptomics in Systemic Vasculitis (CUTIS) (CUTIS)
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03004326 |
Recruitment Status :
Recruiting
First Posted : December 28, 2016
Last Update Posted : January 13, 2023
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Condition or disease |
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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 |
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 approach.
Study Type : | Observational |
Estimated Enrollment : | 50 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | Clinical Transcriptomics in Systemic Vasculitis (CUTIS) |
Actual Study Start Date : | January 2017 |
Estimated Primary Completion Date : | December 2023 |
Estimated Study Completion Date : | December 2023 |

- Evaluation of clinical data and linked biopsy specimens [ Time Frame: 1 year ]Describe cutaneous vasculitis across several different forms of systemic vasculitis using histopathology.
Biospecimen Retention: Samples With DNA

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Ages Eligible for Study: | 5 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
About 56 people with vasculitis will take part in this study at approximately 20 medical centers across North America. Patients with CV, DiV, EGPA, IgA vasculitis, GPA, MPA, PAN, isolated cutaneous vasculitis and urticarial vasculitis will potentially be enrolled into this study.
The protocol will be conducted at the major vasculitis centers in the United States and Canada participating in selected VCRC studies. Skin biopsy specimens collected as standard of care for these diseases will be retrieved and used in research.
Inclusion Criteria:
- Have a cutaneous lesion (purpuric macules, palpable purpura, retiform purpura, nodules, ulcers, or urticarial) believed to be related to active vasculitis
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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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03004326
Contact: Carol McAlear, MA | cmcalear@upenn.edu |
United States, California | |
University of California, Los Angeles | Recruiting |
Los Angeles, California, United States, 90095 | |
Contact: Tandy Ramirez ItandewyRamirez@mednet.ucla.edu | |
United States, Massachusetts | |
Boston University School of Medicine | Completed |
Boston, Massachusetts, United States, 02118 | |
United States, Minnesota | |
Mayo Clinic | Completed |
Rochester, Minnesota, United States, 55905 | |
United States, Ohio | |
Cleveland Clinic | Completed |
Cleveland, Ohio, United States, 44195 | |
United States, Oregon | |
Oregon Health & Science University | Completed |
Portland, Oregon, United States | |
United States, Pennsylvania | |
University of Pennsylvania | Recruiting |
Philadelphia, Pennsylvania, United States, 19104 | |
Contact: Josh Bryer jbryer@pennmedicine.upenn.edu | |
United States, Utah | |
University of Utah | Completed |
Salt Lake City, Utah, United States | |
Canada, Ontario | |
University of Toronto Mount Sinai Hospital | Recruiting |
Toronto, Ontario, Canada, M5G 1X5 | |
Contact: Suneet Khurana suneet.khurana@sinaihealth.ca |
Principal Investigator: | Robert Micheletti, MD | University of Pennsylvania | |
Principal Investigator: | Peter Grayson, MD, MSc | The National Institute of Arthritis and Musculoskeletal and Skin Diseases |
Responsible Party: | Peter Merkel, Chief, Division of Rheumatology Professor of Medicine and Epidemiology, University of Pennsylvania |
ClinicalTrials.gov Identifier: | NCT03004326 |
Other Study ID Numbers: |
VCRC5563 U54AR057319 ( U.S. NIH Grant/Contract ) |
First Posted: | December 28, 2016 Key Record Dates |
Last Update Posted: | January 13, 2023 |
Last Verified: | January 2023 |
DIV CSS EGPA HSP |
GPA MPA PAN Wegeners |
Vasculitis Systemic Vasculitis Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Granulomatosis with Polyangiitis Microscopic Polyangiitis Churg-Strauss Syndrome Polyarteritis Nodosa Vascular Diseases Cardiovascular Diseases Lung Diseases, Interstitial Lung Diseases Respiratory Tract Diseases Autoimmune Diseases |
Immune System Diseases Cerebral Small Vessel Diseases Cerebrovascular Disorders Brain Diseases Central Nervous System Diseases Nervous System Diseases Granuloma Lymphoproliferative Disorders Lymphatic Diseases Arteritis Skin Diseases, Vascular Skin Diseases |