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Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI

Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04856059
Acronym
FIESTA-MRI
Enrollment
300
Registered
2021-04-22
Start date
2021-06-15
Completion date
2029-03-31
Last updated
2026-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fabry Disease

Keywords

Fabry disease, Fabry cardiomyopathy, cardiac MRI, CMR, T1 mapping, T2mapping

Brief summary

This study will evaluate whether cardiac MRI T1 and T2 mapping improves our ability to detect early abnormalities in the heart in patients with Fabry disease and identify patients at increase risk of adverse events.

Detailed description

Fabry disease is an inherited disorder that affects many organs in the body, including the heart. Men and women are both affected, with average life expectancy reduced by 10-20 years. The heart muscle can become thick and scarred in over half of patients, eventually resulting in heart failure, abnormal rhythm and death. The focus of this study will be on improving the detection of early heart disease before irreversible damage has occurred in order to improve patient outcomes. It is hypothesized that new cardiac MRI techniques called T1 and T2 mapping will improve the ability to detect early abnormalities in the heart. Early detection of cardiac disease may enable a personalized treatment approach, potentially improving patient outcomes. The results of the study will identify which patients might benefit from early initiation of treatment to prevent bad outcomes in the future by using cardiac MRI to identify those at higher risk.

Interventions

DIAGNOSTIC_TESTCardiac MRI, ECG/Holter and Blood Biomarkers

Cardiac MRI including T1/T2 mapping, ECG and blood biomarker evaluation will be performed at baseline and follow-up

Sponsors

University Health Network, Toronto
Lead SponsorOTHER
Vancouver General Hospital
CollaboratorOTHER
The Cleveland Clinic
CollaboratorOTHER
Icahn School of Medicine at Mount Sinai
CollaboratorOTHER
IRCCS Policlinico S. Donato
CollaboratorOTHER
Alberta Health services
CollaboratorOTHER
Libin Cardiovascular Institute of Alberta
CollaboratorOTHER
Vancouver Coastal Health
CollaboratorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

cardiac MRI

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Fabry disease; * Age ≥ 18 years.

Exclusion criteria

* History of myocardial infarction; * Contraindication to MRI.

Design outcomes

Primary

MeasureTime frameDescription
Major Adverse Cardiac Events (MACE)5 yearsMACE will be assessed as a composite endpoint defined by the development on one or more of events such as sustained ventricular tachycardia (VT), severe bradycardia, heart failure hospitalization and cardiac death.

Secondary

MeasureTime frameDescription
The FAbry STabilization indEX (FASTEX) score3 yearsFAbry STabilization indEX (FASTEX) score will be evaluated to assess clinical stability or progression of Fabry disease at follow-up. FASTEX score change of ≥20% will be considered an indication of clinical worsening at follow-up. Minimum value 0%. No maximum value. Higher score change indicates worse outcome.

Countries

Canada

Contacts

CONTACTKate Hanneman
kate.hanneman@uhn.ca416-323-6400
PRINCIPAL_INVESTIGATORKate Hanneman

University Health Network, Toronto

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 17, 2026