跳至主要内容
临床试验/NCT01822145
NCT01822145Unknown不适用

PREDICTion of Implantable-Cardioverter Defibrillator Shock Study

Princess Margaret Hospital, Hong Kong1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
ICD-derived T-wave alternans amplitude before ICD shock

研究概览

简要总结

The primary hypothesis is that an ICD shock may be predicted days in advance by a combined score derived from different data obtainable from the ICD

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

入选标准

  • Age ≧ 18 and ≦ 80
  • Patients have documented spontaneous and sustained ventricular arrhythmias in the last six months prior to the enrollment
  • Patients who are in sinus rhythm, have dual-chamber ICD or CRT-D implanted at least one month before enrollment
  • Patients who are in atrial fibrillation, have single-chamber ICD or CRT-D implanted at least one month before enrollment
  • Patients who are compliant to CareLink follow-up

排除标准

  • Patients who are pregnant
  • Patients who are incapable of giving consent to the study
  • Patients who have a life-expectancy of less than 2 years

结局指标

主要结局

ICD-derived T-wave alternans amplitude before ICD shock

时间窗: 6 months

The T-wave alternans amplitude before an ICD shock will be measured in mV and compared to the baseline T-wave alternans amplitude

次要结局

未报告次要终点

研究者

发起方
Princess Margaret Hospital, Hong Kong
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Ngai Yin Chan

Principal investigator

Princess Margaret Hospital, Hong Kong

研究点 (1)

Loading locations...

相似试验