Canadian Network for Autoimmune Liver Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • Observational; no intervention

    Other intervention

    Observational; no intervention

Treatment groups

2,500 Participants
are divided into 1 treatment group
Group A: Observational1 intervention

Trial outcomes

Primary outcomes

1

Liver transplant-free survival over time

Time-to-event

Time frame
Up to 6 years or time of death/liver transplant

Secondary outcomes

1

Biochemical values over time (e.g. aspartate aminotransferase, alkaline phosphatase, alanine aminotransferase, Bilirubin)

Investigate trends of different biochemical values over time

Time frame
Through study completion, an average of 6 months
2

Short Form 36 (SF-36)

Health-Related Quality of Life

Time frame
Through study completion, an average of 6 months
3

PBC-40

Health-Related Quality of Life, specific to Primary Biliary Cholangitis

Time frame
Through study completion, an average of 6 months
4

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

Time frame
Through study completion, an average of 6 months

Other outcomes

Sponsors and contacts

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