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
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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 HospitalVancouver, British Columbia
Canada
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McMaster University Medical Centre
McMaster University Medical CentreHamilton, Ontario
Canada
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Marco Puglia, MD
Toronto General Hospital
Toronto General HospitalToronto, Ontario
Canada
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Royal University Hospital
Royal University HospitalSaskatoon, Saskatchewan
Canada
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University of Alberta Hospital
University of Alberta HospitalEdmonton, Alberta
Canada
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Queen Elizabeth II Health Sciences Centre
Queen Elizabeth II Health Sciences CentreHalifax, Nova Scotia
Canada
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The Ottawa Hospital
The Ottawa HospitalOttawa, Ontario
Canada
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Université de Sherbrooke
Université de SherbrookeSherbrooke, Quebec
Canada
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St. Paul's Hospital
St. Paul's HospitalVancouver, British Columbia
Canada
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Hin Hin Ko, MD
604-688-6332Kingston Health Sciences Centre (HDH Site)
Kingston Health Sciences Centre (HDH Site)Kingston, Ontario
Canada
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McMaster University Medical Centre
McMaster University Medical CentreMontreal, Quebec
Canada
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Marc Deschenes
Foothills Medical Centre
Foothills Medical CentreCalgary, Alberta
Canada
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Health Sciences Centre
Health Sciences CentreWinnipeg, Manitoba
Canada
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London Health Sciences Centre - University Hospital
London Health Sciences Centre - University HospitalLondon, Ontario
Canada
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Centre hospitalier de l'Université de Montréal
Centre hospitalier de l'Université de MontréalMontréal, Quebec
Canada
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- Étude parrainée par
- University Health Network, Toronto
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT03569826