Actively Recruiting

Age: 18Years +
All Genders
NCT05734404

Longitudinal Study for Central Nervous System Vasculitis

Led by University of Pennsylvania · Updated on 2026-01-23

40

Participants Needed

6

Research Sites

408 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

T

The Cleveland Clinic

Collaborating Sponsor

AI-Summary

What this Trial Is About

Primary central nervous system vasculitis (CNSV) is a potentially fatal, single-organ vasculitis that often involves a spectrum of neurologic complications, including strokes, cognitive and speech impairment, visual loss, dementia, and encephalopathy. The purpose of this study is to establish a research cohort to investigate the disease process, treatments, and patient outcomes in CNSV.

CONDITIONS

Official Title

Longitudinal Study for Central Nervous System Vasculitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of primary central nervous system vasculitis confirmed by neurologic deficits
  • Presence of classic angiographic or histopathologic features of angiitis in the central nervous system
  • No evidence of systemic vasculitis or other conditions causing similar features
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Unwillingness to sign informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 6 locations

1

Mayo Clinic

Rochester, Minnesota, United States, 55905

Actively Recruiting

2

Cleveland Clinic

Cleveland, Ohio, United States, 44195

Actively Recruiting

3

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

4

Vanderbilt University

Nashville, Tennessee, United States, 37232

Actively Recruiting

5

St. Joseph's Healthcare

Hamilton, Canada

Actively Recruiting

6

University of Toronto/Sinai Health

Toronto, Canada

Actively Recruiting

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Research Team

C

Carol McAlear

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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