NL-OMON37566撤回不适用
Adaptive CRT optimization at rest and during exercise - AdOpt CRT
Medtronic Trading NL BV0 个研究点目标入组 6 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
- 撤回
- 发起方
- 入组人数
- 6
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
- •* 18 or greater.
- •* sign and date study Informed Consent form.
- •* Subject implanted with a clinically indicated CRT-D device (Medtronic Vision 3D or Protecta models) for at least 1 month but less than 7 months
排除标准
- •* history of persistent or permanent AF
- •* atrial or ventricular tachyarrhythmias or frequent atrial or ventricular ectopy at the time of enrollment.
- •* resting heart rate at the time of enrollment exceeds 90 bpm.
- •* CRT system implanted for more than 7 months
- •* complete AV block.
- •* previous mechanical valve surgeries.
- •* congenital heart disease.
- •* contraindication for an exercise test.
- •* unable to perform a sub-maximal exercise test.
- •* It is not possible to acquire technically acceptable echocardiographic images.
- •* medical conditions that would limit study participation.
- •* Subject is enrolled in the Adaptive CRT study
研究者
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