About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnosis of Primary Biliary Cholangitis and/or Autoimmune Hepatitis
Disqualifiers
Less than 18 years of age
Trial population
Patients with a diagnosis of Primary Biliary Cholangitis and/or Autoimmune Hepatitis across Canada.
Trial design
Cohort
Other
Treatments tested in this trial
Observational; no intervention
Other interventionObservational; no intervention
Treatment groups
Trial outcomes
Primary outcomes
Liver transplant-free survival over time
Time-to-event
Secondary outcomes
Biochemical values over time (e.g. aspartate aminotransferase, alkaline phosphatase, alanine aminotransferase, Bilirubin)
Investigate trends of different biochemical values over time
Short Form 36 (SF-36)
Health-Related Quality of Life
PBC-40
Health-Related Quality of Life, specific to Primary Biliary Cholangitis
5D Pruritus Scale
Itch-Related Quality of Life through 5 dimensions: duration, degree, direction, disability, and distribution. Each dimension is scored from 1(lowest) to 5(highest) for a total score range of 5-25
Sponsors and contacts
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