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Canadian Fabry Disease Initiative (CFDI) National Registry
Sponsor: Canadian Fabry Research Consortium
Summary
CFDI NATIONAL REGISTRY Fabry disease is a rare, inherited, genetic condition due to a deficiency of an enzyme called alpha-galactosidase A. This enzyme deficiency causes the small blood vessels to accumulate a substance called glycolipid. Without sufficient levels of the enzyme, alpha-galactosidase A, persons with Fabry Disease develop severe neuropathic pain, kidney disease, heart disease, stroke and/or premature death; often before the age of 60. Fabry Disease is estimated to affect approximately one out of every 40,000 males and up to twice as many females in Canada. We do not have the exact number of persons in Canada who have this disease. A common problem in studying rare conditions is the difficulty in identifying the majority of people suffering from such a disease. Gathering their health information in order to better understand the natural disease progression and its response to treatment is difficult. Early ERT studies involving humans had small numbers of subjects and the studies were of short duration. The results of these clinical studies did lead to approval of the therapy in many countries around the world including Canada. To date though, evidence of the usefulness of ERT and its direct impact on the natural course of Fabry disease has been limited, while its cost continues to be very high. As a result of these issues, there will need to be continued and long-term collection of information related to the effectiveness of ERT and other treatments to better document its true clinical outcomes in Canadian people with Fabry disease. The Canadian Fabry Disease Initiative National Registry (CFDI-NR) is an observational, voluntary registry designed to collect outcomes data on Fabry disease from people living in Canada.
Official title: Canadian Fabry Disease Initiative National Registry: Outcomes of Rare Disease Therapeutics and Cardiovascular Risk Factor Modification
Key Details
Gender
All
Age Range
5 Years - 85 Years
Study Type
OBSERVATIONAL
Enrollment
600
Start Date
2007-01
Completion Date
2029-10
Last Updated
2024-02-15
Healthy Volunteers
No
Conditions
Interventions
No intervention
This is an observational, voluntary registry.
Locations (5)
Alberta Children's Hospital
Calgary, Alberta, Canada
Vancouver General Hospital Adult Metabolic Diseases Clinic
Vancouver, British Columbia, Canada
Queen Elizabeth II Health Sciences Centre
Halifax, Nova Scotia, Canada
Toronto Western Hospital
Toronto, Ontario, Canada
University of Montreal, Department of Medicine
Montreal, Quebec, Canada