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临床试验/NL-OMON39945
NL-OMON39945已完成不适用

ENHANCED device programming to reduce therapies and improve quality of life in Implantable Cardioverter Defibrillator patients: A prospective, single-arm safety monitoring study - ENHANCED-ICD study

Academisch 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
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

  • Patients implanted with a Medtronic ProtectaTM ICD (VR or DR) or CRT-D, between 18-80 years of age, with a primary or secondary prophylactic indication for ICD therapy according to the current European guidelines, speaking and understanding Dutch, and providing written informed consent will be eligible to participate.

排除标准

  • Patients with a life expectancy less than 1 year, with a history of psychiatric illness other than affective/anxiety disorders, on the waiting list for heart transplantation or with insufficient knowledge of the Dutch language will be excluded.

研究者

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