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临床试验/NCT05776212
NCT05776212招募中不适用

Quantitative-imaging in Cardiac Transthyretin Amyloidosis

University of Edinburgh2 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2021年8月25日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
140
试验地点
2
主要终点
TBR threshold

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

TBR threshold

时间窗: 1.5 years

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

次要结局

  • Change in TBR(2.5 years)
  • TBR threshold(6 months)
  • Change in Cardiac biomarkers(2.5 years)
  • Change in cardiac biomarkers(2.5 years)
  • Change in cardiac indices on CMR(2.5 years)
  • Change in clinical measures(2.5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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