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Canadian Network for Autoimmune Liver Disease

Autoimmune Hepatitis | Overlap Syndrome | Primary Bilary Cirrhosis (PBC)

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.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Diagnosis of Primary Biliary Cholangitis and/or Autoimmune Hepatitis

Exclusion Criteria:

* Less than 18 years of age

Lieu de l'étude

Vancouver General Hospital
Vancouver General Hospital
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Eric M Yoshida, MD

[email protected]
604-875-5371
McMaster University Medical Centre
McMaster University Medical Centre
Hamilton, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Marco Puglia, MD

Toronto General Hospital
Toronto General Hospital
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Bettina Hansen, PhD

[email protected]
416-340-5157
Backup Contact

Kattleya Tirona

[email protected]
Royal University Hospital
Royal University Hospital
Saskatoon, Saskatchewan
Canada

Contactez l'équipe d'étude

Primary Contact

Lawrence Worobetz, MD

[email protected]
306-966-7964
University of Alberta Hospital
University of Alberta Hospital
Edmonton, Alberta
Canada

Contactez l'équipe d'étude

Backup Contact

Ellina Lytvyak

[email protected]
Primary Contact

Andrew Mason, MD

[email protected]
780-492-8176
Queen Elizabeth II Health Sciences Centre
Queen Elizabeth II Health Sciences Centre
Halifax, Nova Scotia
Canada

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The Ottawa Hospital
The Ottawa Hospital
Ottawa, Ontario
Canada

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Backup Contact

Miriam Muir

[email protected]
Primary Contact

Angela Cheung, MD

[email protected]
613-737-8899
Université de Sherbrooke
Université de Sherbrooke
Sherbrooke, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Dusanka Grbic

[email protected]
819-346-1110
Backup Contact

Chantal Guillet

[email protected]
819-346-1110
St. Paul's Hospital
St. Paul's Hospital
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Hin Hin Ko, MD

604-688-6332
Kingston Health Sciences Centre (HDH Site)
Kingston Health Sciences Centre (HDH Site)
Kingston, Ontario
Canada

Contactez l'équipe d'étude

McMaster University Medical Centre
McMaster University Medical Centre
Montreal, Quebec
Canada

Contactez l'équipe d'étude

Backup Contact

Hansi Peiris

[email protected]
514-934-1934
Primary Contact

Marc Deschenes

Foothills Medical Centre
Foothills Medical Centre
Calgary, Alberta
Canada

Contactez l'équipe d'étude

Primary Contact

Mark Swain, MD

[email protected]
403-944-6514
Health Sciences Centre
Health Sciences Centre
Winnipeg, Manitoba
Canada

Contactez l'équipe d'étude

Primary Contact

Nabiha Faisal, MD

[email protected]
204-789-3650
London Health Sciences Centre - University Hospital
London Health Sciences Centre - University Hospital
London, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Karim Qumosani, MD

[email protected]
519-663-3976
Centre hospitalier de l'Université de Montréal
Centre hospitalier de l'Université de Montréal
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Catherine Vincent, MD

[email protected]
514-890-8000
Étude parrainée par
University Health Network, Toronto
Participants recherchés
Plus d'informations
ID de l'étude: NCT03569826