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临床试验/NCT04467411
NCT04467411招募中不适用

Randomised Controlled Study of Physical Exercise Intervention in Breast Cancer Patients at Risk of Anthracycline-induced Cardiomyopathy:The EMBRACE Study

University of Aberdeen1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2020年2月1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
70
试验地点
1
主要终点
Cardiac Energetics

研究概览

简要总结

Cardiomyopathy is a condition that affects the heart muscle, whereby it becomes enlarged, thick or rigid. When the heart muscle becomes involved, it affects the pumping action of the heart. This condition can affect as many as 10% of all patients after undergoing anthracycline cancer drug therapy and unfortunately carries the worst prognosis of all cardiomyopathies. To date, there is no effective intervention that will prevent a patient from developing this condition. The research conducted will look to see if an energy imbalance in the heart predates the onset of detrimental changes to the pumping function of the heart, if this is detected then we can act earlier to prevent the pumping function deteriorating.

详细描述

There is emerging cellular and experimental evidence that cardiac energetic status is reduced after anthracycline treatment, however, this has not been tested in the human heart. The researchers hypothesize that cardiac energetic status is reduced in the human heart after administration of anthracycline therapy in breast cancer patients, inline with the evidence available from all other types of cardiomyopathies. The researchers propose to use in vivo 31Phosphorus cardiac spectroscopy to measure the cardiac energetic status at the beginning and at the end of the cycles of chemotherapy in the hearts of breast cancer patients who are administered epirubicin (the most modern anthracycline to date) and compare this with the cardiac energetic status of age and gender matched healthy controls. Further, the researchers wish to explore if the myopathy-induced effect of anthracyclines extends to the skeletal muscle as well, by examining skeletal muscle biopsies in these patients.

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • A patient who has been diagnosed with breast cancer and has been scheduled for a first cycle of anthracycline therapy.
  • Participant who is willing and able to give informed consent for participation in the study.
  • Healthy (gender and age matched) volunteers willing to give informed consent for participation in the study.

排除标准

  • Contraindication to magnetic resonance scanning such as an implantable cardiac device.

结局指标

主要结局

Cardiac Energetics

时间窗: Through study completion, up to sixteen weeks

Cardiac MRI and MRS

次要结局

  • Blood Biomarkers(Through study completion, up to sixteen weeks)
  • Cardiac Imaging(Through study completion, up to sixteen weeks)
  • Histology(Through study completion, up to sixteen weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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