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