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Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI (FIESTA-MRI)

Primary Purpose

Fabry Disease

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cardiac MRI, ECG/Holter and Blood Biomarkers
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Fabry Disease focused on measuring Fabry disease, Fabry cardiomyopathy, cardiac MRI, CMR, T1 mapping, T2mapping

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Fabry disease;
  • Age ≥ 18 years.

Exclusion Criteria:

  • History of myocardial infarction;
  • Contraindication to MRI.

Sites / Locations

  • University Health NetworkRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Cardiac MRI, ECG and Blood Biomarkers

Arm Description

Additional sequences will be performed during routine clinical cardiac MRI and additional blood samples will be collected during routine blood work.

Outcomes

Primary Outcome Measures

Major Adverse Cardiac Events (MACE)
MACE 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 Outcome Measures

The FAbry STabilization indEX (FASTEX) score
FAbry 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.

Full Information

First Posted
April 20, 2021
Last Updated
July 18, 2023
Sponsor
University Health Network, Toronto
Collaborators
Vancouver General Hospital, The Cleveland Clinic, Icahn School of Medicine at Mount Sinai, Mayo Clinic, University of Colorado, Denver, IRCCS Policlinico S. Donato, Alberta Health services, Libin Cardiovascular Institute of Alberta
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1. Study Identification

Unique Protocol Identification Number
NCT04856059
Brief Title
Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI
Acronym
FIESTA-MRI
Official Title
Fabry Cardiomyopathy: Identification of Early Myocardial Structural and Tissue Abnormalities Using Multiparametric MRI
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 15, 2021 (Actual)
Primary Completion Date
December 31, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Vancouver General Hospital, The Cleveland Clinic, Icahn School of Medicine at Mount Sinai, Mayo Clinic, University of Colorado, Denver, IRCCS Policlinico S. Donato, Alberta Health services, Libin Cardiovascular Institute of Alberta

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fabry Disease
Keywords
Fabry disease, Fabry cardiomyopathy, cardiac MRI, CMR, T1 mapping, T2mapping

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
cardiac MRI
Masking
None (Open Label)
Allocation
N/A
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cardiac MRI, ECG and Blood Biomarkers
Arm Type
Other
Arm Description
Additional sequences will be performed during routine clinical cardiac MRI and additional blood samples will be collected during routine blood work.
Intervention Type
Diagnostic Test
Intervention Name(s)
Cardiac MRI, ECG/Holter and Blood Biomarkers
Intervention Description
Cardiac MRI including T1/T2 mapping, ECG and blood biomarker evaluation will be performed at baseline and follow-up
Primary Outcome Measure Information:
Title
Major Adverse Cardiac Events (MACE)
Description
MACE 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.
Time Frame
5 years
Secondary Outcome Measure Information:
Title
The FAbry STabilization indEX (FASTEX) score
Description
FAbry 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.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fabry disease; Age ≥ 18 years. Exclusion Criteria: History of myocardial infarction; Contraindication to MRI.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kate Hanneman
Phone
416-323-6400
Ext
5521
Email
kate.hanneman@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kate Hanneman
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kate Hanneman, MD
Phone
416-323-6400
Ext
5521
Email
Kate.Hanneman@uhn.ca

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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