跳至主要内容
临床试验/NCT00743522
NCT00743522已完成不适用

Programming Implantable Cardioverter Defibrillators (ICDs) in Patients With Primary Prevention Indication to Prolong Time to First Shock

Abbott Medical Devices1 个研究点 分布在 1 个国家目标入组 1,670 人开始时间: 2008年9月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,670
试验地点
1
主要终点
The primary endpoint of this study is the rate of first shock

研究概览

简要总结

Although shock therapy is effective in terminating ventricular tachycardia (VT), it can be painful to the patient and repetitive shocks can decrease a patient's quality of life. Previous studies have suggested that one or more sets of aggressive device parameter settings may reduce the total number of shocks in primary prevention patients. In addition to shock therapies, antitachycardia pacing (ATP) is also available in ICDs to treat VT. The PROVIDE trial aims to prospectively study the effect of high detection rates, prolonged detection intervals, aggressive SVT discriminators, and extensive ATP therapy in prolonging the time to first shock in primary prevention patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Primary Prevention indication for ICD/ CRT-D

排除标准

  • No prior documented history of spontaneous VT/VF

结局指标

主要结局

The primary endpoint of this study is the rate of first shock

时间窗: Average follow-up period is 530 days

The primary safety endpoint of this study is the rate of arrhythmic syncope

时间窗: Average follow-up period is 530 days

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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