🏛️ Verified NIH Record • Updated 2021-06-04

Canadian Network for Autoimmune Liver Disease (NCT03569826)

🟢 Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: University Health Network, Toronto

🩺 Plain-English Summary (8th-Grade Level)

CaNAL is a longitudinal observational cohort study of patients diagnosed with Primary Biliary Cholangitis (PBC), Autoimmune Hepatitis (AIH), or overlap syndrome. This study creates a nationwide registry and network focusing on high quality long-term follow-up of individual patient data from major Canadian centers. Primary Biliary Cholangitis (PBC) and Autoimmune Hepatitis (AIH) are rare and slowly progressive liver diseases associated with development of cirrhosis, liver cancer (HCC) and liver failure requiring liver transplantation or leading to premature death. The rarity and slowly progressive nature of these autoimmune liver diseases make them difficult to study and only a large scale approach combining patient data from multiple centers across Canada will allow new insights. The primary aim of the Canadian Network for Autoimmune Liver Disease is to build a Canadian registry of patients with PBC, AIH, and overlap syndrome. We capture patient characteristics, laboratory assessments and natural history, patient-reported outcomes including quality of life measures and environmental exposures, response to treatment, and pre- and post-transplant outcomes. We will then identify risk factors associated with critical outcomes for the patient, including response to treatment, progression to transplant, risk of liver cancer, and recurrent disease after transplant. We can identify biomarkers (biochemical indicators of progression of disease) to help diagnose autoimmune liver disease at its earliest stages, ensuring timely treatment and preventing disease progression. CaNAL will provide a better understanding of autoimmune liver diseases, biomarkers predictive of disease progression or non-response to therapy as well as better knowledge of the etiology and pathogenesis. CaNAL will also help to serve as a platform for conducting clinical trials or targeted lab-studies to answer important questions that are unlikely to be evaluated by the pharmaceutical industry.

Who can join: Review the eligibility criteria below.

Location: Foothills Medical Centre — Calgary, Alberta

Age range: 18 Years

🧪 Interventions in This Study

  • Observational; no intervention (OTHER)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (15 Sites)

  • Foothills Medical Centre — Calgary, Alberta
  • University of Alberta Hospital — Edmonton, Alberta
  • Vancouver General Hospital — Vancouver, British Columbia
  • St. Paul's Hospital — Vancouver, British Columbia
  • Health Sciences Centre — Winnipeg, Manitoba
  • Queen Elizabeth II Health Sciences Centre — Halifax, Nova Scotia
  • McMaster University Medical Centre — Hamilton, Ontario
  • Kingston Health Sciences Centre (HDH Site) — Kingston, Ontario
  • London Health Sciences Centre - University Hospital — London, Ontario
  • The Ottawa Hospital — Ottawa, Ontario
  • Toronto General Hospital — Toronto, Ontario
  • Centre hospitalier de l'Université de Montréal — Montreal, Quebec
  • McMaster University Medical Centre — Montreal, Quebec
  • Université de Sherbrooke — Sherbrooke, Quebec
  • Royal University Hospital — Saskatoon, Saskatchewan

📞 Contact the Study Coordinator

Phone: (613) 291-5039

Email: surain.roberts@uhn.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗