Initiative to understand childhood vasculitis
Chronic Childhood Vasculitis: Characterizing the Individual Rare Diseases to Improve Patient Outcomes
This study is trying to gather information and samples from up to 600 children with different types of vasculitis to better understand how the disease affects them and how well treatments are working.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1600 (estimated) |
| Ages | N/A to 20 Years |
| Sex | All |
| Sponsor | University of British Columbia Academic / other |
| Locations | 32 sites (San Francisco, California and 31 other locations) |
| Trial ID | NCT02006134 on ClinicalTrials.gov |
What this trial studies
This initiative aims to collect clinical data and biological samples from up to 600 children diagnosed with various forms of childhood vasculitis, including conditions like Granulomatosis with Polyangiitis and Takayasu Arteritis. The study will gather comprehensive information from medical charts at multiple time points, including diagnosis and follow-up visits, to assess disease activity and treatment outcomes. Additionally, biological samples such as blood, urine, and saliva will be collected to better understand the disease's impact and response to treatment. The initiative is linked to an adult vasculitis study to enhance knowledge across age groups.
Who should consider this trial
Good fit: Ideal candidates include children diagnosed with ANCA-associated vasculitis or other specified forms of vasculitis before the age of 18.
Not a fit: Patients diagnosed with other vasculitis subtypes not included in the study or those over 20 years of age may not benefit from this initiative.
Why it matters
Potential benefit: If successful, this initiative could lead to improved treatment strategies and outcomes for children suffering from vasculitis.
How similar studies have performed: While this initiative builds on existing adult vasculitis studies, it focuses specifically on children, making it a novel approach in this demographic.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
San Francisco, California and 31 other locations
- University of San Francisco — San Francisco, California, United States (Recruiting)
- University of Florida — Gainesville, Florida, United States (Recruiting)
- Comer Children's Hospital — Chicago, Illinois, United States (Recruiting)
- Riley Hospital for Children — Indianapolis, Indiana, United States (Recruiting)
- The Joseph M. Sanzari Children's Hospital — Hackensack, New Jersey, United States (Recruiting)
- Children's Hospital at Montefiore — Bronx, New York, United States (Recruiting)
- Akron Children's Hospital — Akron, Ohio, United States (Recruiting)
- Texas Children's Hospital — Houston, Texas, United States (Recruiting)
- University of Utah / Primary Children's Hospital — Salt Lake City, Utah, United States (Recruiting)
- Seattle Children's Hospital — Seattle, Washington, United States (Recruiting)
- University of Calgary / Alberta Children's Hospital — Calgary, Alberta, Canada (Recruiting)
- BC Children's Hospital — Vancouver, British Columbia, Canada (Recruiting)
- Janeway Childrens Health and Rehabilitation Centre — St. John's, Newfoundland and Labrador, Canada (Active_not_recruiting)
- IIWK Health Centre — Halifax, Nova Scotia, Canada (Recruiting)
- London Health Sciences Centre — London, Ontario, Canada (Recruiting)
- Children's Hospital of Eastern Ontario — Ottawa, Ontario, Canada (Recruiting)
- Hospital for Sick Children — Toronto, Ontario, Canada (Completed)
- Royal University Hospital — Saskatoon, Saskatchewan, Canada (Completed)
- Rigshospitalet — Copenhagen, Denmark (Completed)
- University Children's Hospital — Munster, Germany (Active_not_recruiting)
- Sanjay Gandhi Post Graduate Institute — Lucknow, India (Recruiting)
- Siriraj Hospital — Bangkok, Thailand (Recruiting)
- Birmingham Children's Hospital NHS Foundation Trust — Birmingham, United Kingdom (Recruiting)
- Royal Hospital for Children — Glasgow, United Kingdom (Recruiting)
- Leeds Children's Hospital — Leeds, United Kingdom (Recruiting)
- Alder Hey Children's Hospital — Liverpool, United Kingdom (Recruiting)
- Royal Manchester Children's Hospital — Manchester, United Kingdom (Recruiting)
- Great North Children's Hospital — Newcastle upon Tyne, United Kingdom (Recruiting)
- Nottingham Children's Hospital — Nottingham, United Kingdom (Recruiting)
- Nuffield Orthopaedic Centre — Oxford, United Kingdom (Recruiting)
- Sheffield Children's Foundation Trust — Sheffield, United Kingdom (Recruiting)
- Southampton General Hospital — Southampton, United Kingdom (Recruiting)
Study contacts
- Principal investigator: David Cabral, MBBS — University of British Columbia; BC Children's Hospital
- Study coordinator: Else S. Bosman, PhD
- Email: pedvas@cw.bc.ca
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.