跳至主要内容
临床试验/NL-OMON32196
NL-OMON32196已完成不适用

E-pot Study: EnSite & Pressure- Volume in Cardiac Resynchronization Therapy, a multicenter, prospective, feasability, non-randomized pilot study - E-pot study

St. Jude Medical0 个研究点目标入组 30 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
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • •CRT-D conventional indication
  • •QRS width > 120 ms
  • •Left Ventricular Ejection Fraction (LVEF) < 35%.
  • •Left Bundle Branch Block (LBBB)
  • •MI documented by echo or MRI
  • •Cardiomyopathy stable for the last Month (or longer)
  • •Pharmacological treatment unchanged during the 3 last Months (or longer)
  • •Heart failure NYHA class II & III

排除标准

  • •History of chronic AF
  • •MI within the last 3 Months
  • •Previous pacemaker or ICD implanted
  • •Claudication intermittens or other significant arterial vein issues in the aortic-iliac route
  • •Moderate to severe aortic valve stenosis or indication for valve surgery or mechanical aortic valve replacement or thrombus in Left Ventricle
  • •Age <18 years or > 80 years
  • •Heart failure NYHA class IV
  • •Serious comorbidity such as cancer, with a likelihood of death during the study
  • •Unwilling or unable to sign the consent form for participation
  • •Females of childbearing age not using medically prescribed contraceptives

研究者

相似试验

E-pot Study: EnSite & Pressure- Volume in Cardiac... | 临床试验