NCT00832260已完成不适用
Influence of Atrial Pulse Width in the Behaviour of ACap™ Confirm Algorithm.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 主要终点
- Percentage of Patients in Whom ACap™ Confirm Algorithm is Programmed Safely to ON During the First 12 Months.
研究概览
简要总结
The purpose of this observational study is to collect data regarding the population of patients with a pacemaker implanted.
详细描述
The purpose of this observational study is to collect data regarding the population of patients whit a Zephyr™ pacemaker implanted, models 5826 and 5820, and active or passive fixation leads , when the Algorithms Acap Confirm, which automatically regulates the Atrial Pulse Width, is enabled.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 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
- •Patient has an indication for implantation of a dual-chamber pacemaker;
- •Patient is older than 18 years of age
- •Patient has signed the study specific Informed consent document.
- •Primo implant.
排除标准
- •Patient is pregnant or nursing
- •Patient is less than 18 years of age
- •Patient is in New York Heart Association (NYHA) class III and IV.
- •Patient has a pacemaker replacement;
- •Patient is unable to attend the follow-up visits;
结局指标
主要结局
Percentage of Patients in Whom ACap™ Confirm Algorithm is Programmed Safely to ON During the First 12 Months.
时间窗: 12 months
次要结局
- Percentage of Patients in Whom ACap™ Confirm Algorithm is Recommended at a Pulse Width of 0.4 Milliseconds (ms) During All Follow-ups (Implant, Staples Removal, 3, 6, 9 and 12 Months).(12 months)
研究者
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