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临床试验/NCT00606775
NCT00606775Unknown4 期

Carvedilol for the Prevention of Minor Cardiac Damage and Cardiac Function in Duchenne Muscular Dystrophy

Suzuka Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2007年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
60
试验地点
1
主要终点
The suppression of minor cardiac damage indicated as elevation of plasma cTnI

研究概览

简要总结

Purpose This cardiac dysfunction in patients with Duchenne muscular dystrophy is associated with minor cardiac damage as indicated by elevation of plasma cardiac troponin I (cTnI). The purpose of this study is to investigate whether the administration of Carvedilol can suppress the minor cardiac damage and prevent deterioration of cardiac function.

详细描述

The life span in patients with Duchenne muscular dystrophy has been extending due to the development of artificial respiratory devices. According to that, the ratio of cardiac dysfunction as a cause of death has been increasing. This cardiac dysfunction was associated with minor cardiac damage as indicated by elevation of plasma cardiac troponin I (cTnI). Furthermore, and the detection rate of cTnI plasma as revealed to be correlated with the deterioration speed of LV dysfunction assessed by serial echocardiography measurements. Accordingly, if this minor cardiac damage is suppressed, it is postulated that the progression of cardiac dysfunction can be stopped. In the cases with ventricular arrhythmia and tachycardia, we found plasma cTnI became undetectable after administration of beta-blocker. Accordingly, we investigate whether administration of beta-blocker, carvedilol can persistently suppress the minor cardiac damage and lead to suppress the deterioration of LV function. Note that his study preventive study for preserved to moderate LV dysfunction and is not intended to the beta-blocker treatment for severe LV dysfunction. Because we assume that the mechanism of elevation of cTnI is different; spontaneous in preserved to mild LV dysfunction in patients but LV wall stress in severe LV dysfunction in patients with Duchenne muscular dystrophy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
8 Years 至 45 Years(Child, Adult)
性别
Male
接受健康志愿者

入选标准

  • Male patients with Duchenne muscular dystrophy are required to meet the following criteria:
  • Aged 8 to 45 years
  • Positive plasma cardiac troponin I (0.06ng/mL) at least 4 blood measurement in every 3 month.
  • Left ventricular ejection fraction >30% by echocardiography assessment
  • Written informed consent

排除标准

  • Patients with the following conditions will be excluded from the study:
  • Left ventricular ejection fraction <30%
  • No plasma cTnI elevation
  • beta-blocker is already administered without measurement of plasma cTnI
  • Contraindication against treatment with β blockers
  • Any other serious disease that could potentially complicate the management and follow-up protocols

研究组 & 干预措施

Carvedilol

Experimental

干预措施: Carvedilol (Drug)

结局指标

主要结局

The suppression of minor cardiac damage indicated as elevation of plasma cTnI

时间窗: 2 years

次要结局

  • Left ventricular function deterioration assessed by echocardiography In-hospital mortality for cardiac dysfunction In-hospital mortality for any cause Overall mortality(5 years)

研究者

发起方
Suzuka Hospital
申办方类型
Other Gov

研究点 (1)

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