跳至主要内容
临床试验/NL-OMON37928
NL-OMON37928已完成不适用

High Intensity Interval Training after Cardiac Resynchronization Therapy: a randomised controlled trial - HIT-CRT

Maxima Medisch Centrum0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • •-Written informed consent.
  • •-Systolic heart failure due to ischemic cardiomyopathy (due to one or more myocardial infarction, as confirmed with echocardiography) or dilating cardiomyopathy (no history of myocardial infarction, no proven ischemia, no congenital heart disease and no severe valve disorder)
  • •-Left ventricular ejection fraction < 35% before CRT.
  • •- New York Heart Association (NYHA) classII or III before CRT

排除标准

  • •* Myocardial infarction or unstable angina less than 3 months prior to inclusion
  • •* Clinical signs of decompensated heart failure
  • •* Ventricular tachycardia or ischemia during exercise
  • •* Participation in a training program (*2/week) in the last year
  • •* Intracardiac shunts or congenital heart disease limiting exercise capacity
  • •* Orthopaedic, vascular, pulmonary, neuromuscular and other disease limiting exercise capacity
  • •* Pathological Allen test , In casu no sufficient collateral circulation to the hand, in case of radial artery cannulation.

研究者

发起方
Maxima Medisch Centrum

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