Vascular Tissue Collection for Vasculitis Research

VCRC Tissue Repository

Recruiting Observational Study
Aortitis Cutaneous Vasculitis Eosinophilic Granulomatosis With Polyangiitis Giant Cell Arteritis Granulomatosis With Polyangiitis (Wegener's) Henoch-Schonlein Purpura IgA Vasculitis Microscopic Polyangiitis Polyarteritis Nodosa Takayasu Arteritis Churg-Strauss Syndrome
No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
University of Pennsylvania · Other
Who this trial is looking for

This trial is looking for participants who have been part of other studies related to vasculitis. Participation involves allowing researchers to use tissue samples for research purposes.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am part of another VCRC study.

You may not be able to join if

  • I cannot give informed consent.
  • I am unwilling to allow the use of my tissue for research.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial
The purpose of this study is to collect existing tissue specimens from subjects enrolled in Vasculitis Clinical Research Consortium (VCRC) studies. Analysis of these tissue specimens and linked clinical data collected through VCRC studies may lead to the identification and development of a series of translational research projects. Results of these studies will provide vasculitis researchers with …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * A participant will be deemed eligible for this study if the participant is/was enrolled in another one of the VCRC observational/longitudinal protocols (5502, 5503, 5504, 5505, 5506, 5507, 5563) and/or one of the VCRC interventional studies (5522, 5523, 5526, 5527, or 5562). …
Contacts