跳至主要内容
临床试验/NCT00848341
NCT00848341已完成不适用

Canadian Registry of ICD Implant Testing Procedures

Guidant Corporation0 个研究点目标入组 261 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
261
主要终点
to systematically collect and quanitfy characteristics of ICD implant procedures in Canadian Hospitals

研究概览

简要总结

To document practices in Canadian ICD implant centres around defibrillation therapy efficacy testing.

详细描述

To document types of defibrillation testing (DFT) procedures are in current use in Canada, rates of use an dno use of DFT testing, medical indications for non use of DFT testing, rate of successful testing of first lead configuration, rates and types of complications from DFT testing, costs of implant procedures and the costs associated with DFT testing, short term outcomes of patients with different types of implant procedures.

研究设计

研究类型
Observational
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

入选标准

  • Receiving a Guidant ICD system, including replacements

排除标准

  • New epicardial lead(s) implanted, included in another cardiovascular trial (may be in the ELECTION Study)

结局指标

主要结局

to systematically collect and quanitfy characteristics of ICD implant procedures in Canadian Hospitals

时间窗: 3 years

次要结局

未报告次要终点

研究者

申办方类型
Industry

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Canadian Registry of ICD Implant Testing Procedures | 临床试验