跳至主要内容
临床试验/NCT06173089
NCT06173089招募中不适用

REmote MOnitoring of paTiEnts witH pacEmaker or implAntable cardioverteR defibrillaTor

Semmelweis University Heart and Vascular Center1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 2023年1月30日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
800
试验地点
1
主要终点
The composite of all-cause mortality, heart failure events

研究概览

简要总结

However, the current guidelines recommend the use of remote monitoring (RM) in patients with cardiac implantable electronic devices (CIED) to reduce inappropriate shocks or early detection of atrial fibrillation, data is incomprehensive on the effectiveness of decreasing heart failure events or mortality in patients with heart failure and reduced ejection fraction (HFrEF). The only randomized trial, which proved the efficacy of RM on mortality was the IN-TIME trial, which used a strict protocol for detection and intervention of the heart failure events.

The primary aim of this study is to optimize the use of remote monitoring system in HFrEF patients already implanted an implantable cardiac defibrillator (ICD) or a cardiac resynchronization therapy (CRT). By creating a high-quality system with structured safety-net, which is able to use the data of remote monitoring messages and alerts of our patients, we can improve their outcome. The primary endpoint is the non-fatal heart failure event or all-cause mortality. Secondary outcomes include all-cause mortality, cardiovascular mortality, heart failure hospitalization, cardiovascular hospitalization, unscheduled visits, af burden, stroke, inappropriate shocks, quality of life, NYHA functional class.

By using artificial intelligence-based methods, the optimal cut-off values of the previously, empirically used alert parameters will be validated or challenged. Additionally, cost-effectiveness to reduce the hospitalizations will be calculated.

Due to this remote monitoring structured safety-net, these patients with severe heart failure can be treated more efficiently, safely and cost-effectively.

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 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • CRT-P/CRT-D patients with a feasible device for home monitoring
  • ICD (VVI/VDD/DDD) patients with a feasible device for home monitoring
  • Transmission performance >80% in the first 2 weeks with new device
  • Informed consent

排除标准

  • Life expectancy<1 year
  • Unable to transmit data
  • Patient is unable to visit the physician/clinic in 12 hours when it is indicated by the alerts
  • Expected non-compliance
  • Known drug, alcohol abuse
  • Participation in other study or HM system concept

结局指标

主要结局

The composite of all-cause mortality, heart failure events

时间窗: 12 months

次要结局

  • cardiovascular hospitalization(12 months)
  • cardiovascular mortality(12 months)
  • unscheduled visits(12 months)

研究者

发起方
Semmelweis University Heart and Vascular Center
申办方类型
Other
责任方
Sponsor

研究点 (1)

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