Pediatric Vasculitis Initiative
Launched by UNIVERSITY OF BRITISH COLUMBIA · Dec 4, 2013
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The Pediatric Vasculitis Initiative is a research study focused on understanding rare and serious blood vessel diseases in children, such as Granulomatosis With Polyangiitis and Takayasu Arteritis. These conditions can cause inflammation in important organs like the kidneys and lungs, and while some children may experience milder symptoms that can be treated with safer medications, others may need stronger treatments that could have serious side effects. The goal of this trial is to collect information from children diagnosed with these diseases to better classify their conditions, understand the best treatment options, and identify any potential risks associated with those treatments.
To participate, children must have been diagnosed with one of the targeted types of vasculitis before the age of 18. Healthy children and adults can also join as control participants, but certain health conditions may exclude them. Participants will contribute data through an online registry, which will help researchers gather enough information to improve how these diseases are diagnosed and treated in children. Additionally, samples like blood and tissue will be collected for laboratory studies to help find better ways to identify and manage these conditions in the future.
Gender
ALL
Eligibility criteria
- Inclusion criteria for vasculitis subjects:
- • Diagnosed with ANCA-associated vasculitis (AAV: such as Granulomatosis with Polyangiitis (GPA), Eosinophilic Granulomatosis with Polyangiitis (EGPA) and Microscopic Polyangiitis (MPA)), Primary Angiitis of the Central Nervous System (PACNS), Unclassified vasculitis, Takayasu's Arteritis (TA) or Polyarteritis Nodosa (PAN) before age 18
- Inclusion criteria for healthy controls:
- • Healthy adult or child
- Exclusion Criteria for vasculitis subjects:
- • Diagnosed with other vasculitis subtypes not listed above
- • More than 20 years of age
- Exclusion criteria for healthy controls:
- • Donated greater than 20 ml of blood in the previous three weeks
- • Has an immune disorder or blood borne infectious diseases (such as HIV or Hepatitis)
- • Has vasculitis, multiple sclerosis, diabetes, an autoimmune disease, a thyroid condition, or other chronic conditions involving the heart, lungs, gut or kidney
- • Has a previous history of anaemia or abnormal blood clotting
- • Has a current or previous drug abuse problem
About University Of British Columbia
The University of British Columbia (UBC) is a leading research institution located in Vancouver, Canada, renowned for its commitment to advancing health sciences through innovative research and education. As a prominent clinical trial sponsor, UBC leverages its interdisciplinary expertise and state-of-the-art facilities to conduct rigorous clinical studies aimed at improving patient outcomes across various medical fields. The university fosters collaborations with healthcare professionals, industry partners, and community stakeholders to translate research findings into practical applications, thereby contributing to the global advancement of medicine and public health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Copenhagen, , Denmark
Ottawa, Ontario, Canada
Saskatoon, Saskatchewan, Canada
Gainesville, Florida, United States
Louisville, Kentucky, United States
Houston, Texas, United States
Manchester, , United Kingdom
Toronto, Ontario, Canada
Augusta, Georgia, United States
Akron, Ohio, United States
Barcelona, , Spain
Southampton, , United Kingdom
Indianapolis, Indiana, United States
Bangkok, , Thailand
Vancouver, British Columbia, Canada
Seattle, Washington, United States
Belgrade, , Serbia
Liverpool, , United Kingdom
Birmingham, , United Kingdom
Bronx, New York, United States
London, Ontario, Canada
San Francisco, California, United States
Chicago, Illinois, United States
Hackensack, New Jersey, United States
Salt Lake City, Utah, United States
Buenos Aires, , Argentina
Calgary, Alberta, Canada
St. John's, Newfoundland And Labrador, Canada
Halifax, Nova Scotia, Canada
Munster, , Germany
Lucknow, , India
Florence, , Italy
Coyoacán, , Mexico
Saint Petersburg, , Russian Federation
Glasgow, , United Kingdom
Leeds, , United Kingdom
Newcastle Upon Tyne, , United Kingdom
Nottingham, , United Kingdom
Oxford, , United Kingdom
Sheffield, , United Kingdom
Patients applied
Trial Officials
David Cabral, MBBS
Principal Investigator
University of British Columbia; BC Children's Hospital
Raashid Luqmani, DM FRCP(E)
Principal Investigator
University of Oxford
Dirk Foell, MD
Principal Investigator
Universität Münster
Robert Hancock, PhD
Principal Investigator
University of British Columbia
Colin Ross, PhD
Principal Investigator
University of British Columbia
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials