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NCT Number: NCT05776212

Quantitative-imaging in Cardiac Transthyretin Amyloidosis

Transthyretin amyloid cardiomyopathy (ATTR-CM), is a heart muscle disease that's stops the heart muscle working properly. With an ageing population, it is increasingly common but untreated, it has a poor prognosis. Several novel expensive treatments have become available, although we do not understand exactly how they work and why some patients respond, and others do not. The challenge is to develop better methods for monitoring the effects of these treatments, maximizing their benefits and cost-effectiveness. In I-CARE we aim to bring a new imaging technique, named 18F-fluoride PET, to the clinic and thereby improve the care of patients with ATTR-CM.

Hypotheses:

1. A delayed imaging protocol and state-of-the-art PET motion correction will optimise 18F-fluoride imaging in ATTR-CM and provide a clear threshold in myocardial TBR values for the diagnosis of ATTR-CM. 2. Optimised 18F-fluoride PET will provide a quantitative marker of the ATTR-CM burden that will allow disease progression and treatment response to be tracked. 3. Myocardial 18F-fluoride TBR values will reduce in patients responding to tafamidis treatment and increase in non-responders and patients not receiving therapy

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Medical Centre Groningen

Groningen, 9713 GZ, Netherlands

Location status: Recruiting

Location contact

Riemer HJ Slart, MD PhD

CONTACT

[email protected]

+31 50 361 1835

About this study

Studies have shown that there is calcium deposition in the heart muscle in ATTR-CM but exactly how this happens is not completely understood. Tafamidis, a new drug treatment, has shown improved outcomes for patients with ATTRCM by reducing hospitalisations and improving survival but the mechanism of action of Tafamidis is also not clearly understood yet. 18F-Fluoride PET/CT offers the opportunity to study this phenomenon of calcium deposition in ATTR-CM in more detail and study and track response to the new drug treatment. This will also provide an opportunity to investigate whether tafamidis therapy reduces calcium deposition in the heart muscle associated with ATTR-CM.

We have designed the study specifically to answer our research questions as best as possible, whilst keeping burdens to the patients at a minimum.

To the best of our knowledge this will be the first human study to utilise this imaging technique to assess and track response to the new drug treatment in ATTR-CM. We hope that it will provide major insights in to complex interactions at play, that could drive forward the development of novel therapeutic strategies for patients with ATTR-CM.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Completion of informed consent
  • Age > 40 years for patients with ATTR or AL cardiac amyloidosis and age >30 years for 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 criteria

  • Inability or unwilling to give informed consent
  • Women who are pregnant, breastfeeding or of child-bearing potential (women who have experienced menarche, are pre-menopausal and have not been sterilised) will not be enrolled 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

Treatment and study plan

18F-fluoride PET

Radiation

Positron emission tomography using 18F-fluoride as a tracer

Primary outcomes

  1. TBR threshold

    Time frame: 1.5 years

    Tissue to background ratio with a good specificity and sensitivity to differentiatie subjects with ATTR-CM from subjects with phenocopies.

Secondary outcomes

  1. Change in TBR

    Time frame: 2.5 years

    Change in TBR on 18F-fluoride PET/CT during one year of follow up.

  2. Change in cardiac indices on CMR

    Time frame: 2.5 years

    Change in cardiac indices on magnetic resonance imaging, such as left ventricular ejection fraction

  3. Change in cardiac biomarkers

    Time frame: 2.5 years

    Change in NT-ProBNP during one year of follow up.

  4. Change in clinical measures

    Time frame: 2.5 years

    Change in clinical measures such as 6-minute walk test

  5. TBR threshold

    Time frame: 6 months

    Specificity and sensitivity of TBR thresholds at different scanning times.

  6. Change in Cardiac biomarkers

    Time frame: 2.5 years

    Change in cardiac high sensitivity troponin I during 1 year of follow up

  7. Change in clinical measures

    Time frame: 2.5 years

    Change in KCCQ score during 1 year of follow up

  8. Change in cardiac indices on CMR

    Time frame: 2.5 years

    change in left ventricular mass at 1 year follow up

  9. Change in cardiac indices on CMR

    Time frame: 2.5 years

    change in extracellular volume at 1 year follow up

  10. Change in cardiac indices on CMR

    Time frame: 2.5 years

    Change in left ventricular global longitudinal strain at 1 year follow up

Study contacts

Contact information is provided by the study sponsor or research team.

Riemer Slart, MD PhD

CONTACT

[email protected]

+31503611835

Sponsors and collaborators

Lead sponsor

University of Edinburgh

Other

Collaborators

  • British Heart Foundation
  • Deutsches Zentrum für Herz-Kreislauf-Forschung (DZHK)
  • Netherlands Heart Foundation

Registry information

Acronym: I-CARE

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Mar 20, 2023
Registry last updated
Jun 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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