Impact of Agalsidase Alfa Therapy on Cardiac funcTION in Patients With Fabry's Cardiomyopathy (ACTION-Fabry Trial)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 25
- 试验地点
- 1
- 主要终点
- global longitudinal strain
研究概览
简要总结
Study Design: This is an observational study. No treatment or intervention will be assigned to the subjects. All patients will receive full standard of care concomitant medication for the treatment of their cardiac condition. 25 patients with genetically confirmed Anderson-Fabry disease who have a plan to start ERT with Agalsidase Alfa will undergo 2D strain, diastolic stress echocardiography, LV vortex flow analysis, and CMR at baseline and after 1 year of treatment with ERT with Agalsidase Alfa for follow-up.
详细描述
- Objectives - The purpose of this study is to evaluate the impact of ERT with Agalsidase Alfa on LV diastolic function and flow in patients with Fabry's cardiomyopathy using LV 2D strain, diastolic stress echocardiography, LV vortex flow and CMR.
- Primary / Secondary Endpoint 1) Primary endpoint:
-
Change from baseline in peak exercise E/E' by diastolic stress echocardiography, global longitudinal strain and LV vortex flow parameters at 1 year 2) Secondary endpoints:
-
Changes from baseline in extracellular volume by CMR (T1 mapping) at 1 year follow up
-
Changes from baseline in evaluation of the degree of the resting LV diastolic function
-
Changes from baseline in other echo-parameters; LV mass index, reduction of peak exercise E/E prime at 1 year follow up
-
Changes from baseline in quality of life using questionnaire ⑤ Change from baseline in peak VO2, exercise time, AT by diastolic stress echocardiography at 1 year follow up ⑥ Change in T1 baseline (myo, ms) & T1 baseline (blood, ms), T1 postcontrast (myo, ms) & T1 baseline (blood, ms) by CMR
- Study Methods 1) Study Design: This is an observational study. No treatment or intervention will be assigned to the subjects. All patients will receive full standard of care concomitant medication for the treatment of their cardiac condition. 25 patients with genetically confirmed Anderson-Fabry disease who have a plan to start ERT with Agalsidase Alfa will undergo 2D strain, diastolic stress echocardiography, LV vortex flow analysis, and CMR at baseline and after 1 year of treatment with ERT with Agalsidase Alfa for follow-up.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 16 Years 至 75 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients aged 16~ 75 years with Fabry disease confirmed by enzyme assay and gene test
- •Patients who have LVH in 2D echocardiography (end diastolic septum and posterior wall thickness ≥ 12mm) or Patients who present with cardiac changes (indicative of disease progression such as decreased global longitudinal strain on 2D strain echocardiography or low native T1 mapping on CMR)
- •Patients provided written informed consent to participate in this study
排除标准
- •Contraindication for enzyme replacement treatment with Agalsidase Alfa
- •Patients who cannot receive supine bicycle stress echocardiography, contrast echocardiography or CMR
- •Patients with hemodynamically significant valvular heart disease or arrhythmias
- •Patients who have history of acute myocardial infarction or congestive heart failure with reduced LV ejection fraction of less than 35%
- •Patients who had any cerebrovascular accident in the prior 6 months
- •Scheduled or planned surgery in the next 6 months
- •Patients with chronic liver cirrhosis
- •Patients who are allergic to contrast agent (e.g. Definity�, Lantheus Medical Imaging, North Billerica, MA, USA)
结局指标
主要结局
global longitudinal strain
时间窗: 1 year
peak exercise E/E' by diastolic stress echocardiography
时间窗: 1 year
Change from baseline in peak exercise E/E' by diastolic stress echocardiography
次要结局
- extracellular volume by CMR(1 year)
- quality of life using questionnaire(1 year)
- evaluation of the degree of the resting LV diastolic function(1 year)