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Clinical Trials/NCT06409585
NCT06409585
Recruiting
Not Applicable

Cardiomyopathies and Heart Muscle Diseases: Cardiac Imaging in the Evaluation of Myocardial Fibrosis Transition

University of Edinburgh1 site in 1 country290 target enrollmentMay 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure With Preserved Ejection Fraction
Sponsor
University of Edinburgh
Enrollment
290
Locations
1
Primary Endpoint
Target-to-background ratio
Status
Recruiting
Last Updated
8 months ago

Overview

Brief Summary

Heart scarring, also known as fibrosis, plays a major role in a lot of heart muscle abnormalities. These abnormalities of the heart muscle can lead to major issues such as symptoms of heart failure, dangerous heart rhythm disturbances and even death. However, a lot of these conditions are still not fully understood and treatment options are limited. We here aim to use a new radioactive dye called 68Ga-FAPI to identify patterns and the activity of heart muscle scarring. This radioactive dye is being used in humans particularly in identifying and monitoring cancers and has shown promise in identifying scarring in the heart as well. This will help us not only understand the underlying disease process and risk stratify these patients but also potentially help us develop new targeted therapies that can affect heart muscle scarring. Participants will undergo a baseline MRI scan using this new dye and a plain MRI scan will repeated 12-18 months after to see if there are any changes in the process.

Registry
clinicaltrials.gov
Start Date
May 1, 2023
End Date
January 1, 2028
Last Updated
8 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • HFpEF cohort
  • Male or female between 30 to 90 years old
  • Provision of informed consent prior to any study specific procedures
  • Patients with symptomatic heart failure with preserved ejection fraction as defined by the presence of heart failure symptoms (dyspnoea, reduced exercise tolerance, fatigue), signs (elevated jugular venous pressure, pulmonary crackles, peripheral oedema) as well as echocardiographic features (preserved left ventricular systolic function (\>50%) and reduced diastolic function with septal e' \<7cm/s or lateral e' \<10cm/s).
  • Hypertrophic cardiomyopathy cohort
  • Male or female between 30 to 90 years old
  • Provision of informed consent prior to any study specific procedures
  • Established diagnosis of hypertrophic cardiomyopathy: left ventricular wall thickness \>15mm by any imaging modality without a loading condition to explain the hypertrophy OR
  • Left ventricular wall thickness of \>13 mm by any imaging modality in the presence of a genetic or non-genetic component, supported by other features including family history, non-cardiac symptoms, ECG changes and laboratory tests.
  • Hypertensive heart disease cohort

Exclusion Criteria

  • Inability or unwilling to give informed consent.
  • History of claustrophobia or inability to tolerate supine position for the PET/MR or PET/CT scans.
  • Impaired renal function with eGFR of \<30 mL/min/1.73 m
  • Women who are pregnant or breastfeeding.
  • Iodine or gadolinium contrast allergy
  • Contra-indication to CT scanning

Outcomes

Primary Outcomes

Target-to-background ratio

Time Frame: 1-2 years

Standardised uptake values

Time Frame: 1-2 years

Study Sites (1)

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