Understanding Vasculitis: An Observational Study
This study aims to better understand idiopathic systemic vasculitis, a group of diseases like Takayasu's Arteritis and Giant Cell Arteritis, where blood vessels become inflamed and damaged. Researchers want to learn more about the signs, symptoms, and genetic factors that influence these conditions. They are also looking for ways to predict how the disease might progress over time. You may be able to join if you are age 3 or older and have vasculitis, are suspected of having it, or are a healthy volunteer. This is an observational study, meaning no specific treatments are being tested; instead, researchers will gather information about your condition to help improve future care.
- Study design
- This is an observational study designed to enroll up to 4000 participants. It is not testing a specific intervention but rather collecting information about vasculitis.
- What's involved
- Participants will be evaluated by a doctor specializing in vasculitis and will provide a blood sample.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary goal is to study the disease's characteristics, measured at the end of the study. The duration of follow-up is not specified.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Studies of the Natural History, Pathogenesis, and Outcome of Idiopathic Systemic Vasculitis
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Peter C Grayson, M.D. · PRINCIPAL_INVESTIGATOR · National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- To study the pathogenesis of patients affected with idiopathic systemic vasculitis, including clinical, radiographic, immunological, and genetic characteristics of the diseaseend of study
To study the pathogenesis of patients affected with idiopathic systemic vasculitis, including clinical, radiographic, immunological, and genetic characteristics of the disease