Phase
Condition
Amyloidosis
Treatment
18F-fluoride PET
Clinical Study ID
Ages > 40 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Completion of informed consent
Age > 40 years for patients with ATTR or AL cardiac amyloidosis and age >30 yearsfor patients with HCM
ATTR cardiac amyloid according to Expert Consensus Recommendations
AL amyloidosis according to Expert Consensus Recommendations
Hypertrophic cardiomyopathy according to European Society of Cardiology guidelines
Exclusion
Exclusion Criteria:
Inability or unwilling to give informed consent
Women who are pregnant, breastfeeding or of child-bearing potential (women who haveexperienced menarche, are pre-menopausal and have not been sterilised) will not beenrolled into the trial.
Renal dysfunction (eGFR ≤30 mL/min/1.73m2)
NYHA Class IV heart failure
Patients with atrial fibrillation and poor rate control.
Contraindications to MR
Previous history of contrast allergy of adverse reactions (gadolinium)
Contraindications to tafamidis therapy
Study Design
Study Description
Connect with a study center
University Medical Centre Groningen
Groningen, 9713 GZ
NetherlandsActive - Recruiting
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