NL-OMON36274已完成不适用
Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of Chronic Heart Failure - DEFEAT-HF
Medtronic Trading NL BV0 个研究点目标入组 10 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
- 发起方
- 入组人数
- 10
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
- •LVEF of 35% or less
- •NYHA functional Class III
- •QRS duration less than 120 ms
- •LVEDD of 55 mm - 80 mm
- •Receiving stable medical therapy for heart failure prior to enrollment.
排除标准
- •Temporal stop of anticoagulation therapy poses an unacceptable health risk
- •Inability to perform an exercise capacity test
- •Pregnancy or likely to get pregant during the course of the study
- •CABG/PCI/BMS procedures within the past 90 days
- •Heart transplant
- •Acute Coronary Syndrome within the past 90 days
- •Congenital heart disease with significant hemodynamic shunting
- •Reversible cardiomyopathy (i.e. tachycardia induced heart failure)
- •Diagnosed unstable angina pectoris
- •Unstable coronary artery disease
- •CRT device implanted
- •non-Medtronic ICD, pacemaker or defibrillation lead
- •Patient already has a neurostimulator
- •(see p15-16)
研究者
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