跳至主要内容
临床试验/CTRI/2009/091/001071
CTRI/2009/091/001071
已完成
4 期

Shock-Less study: A prospective, non-randomized, multi-centre post market clinical trial.

India Medtronic Pvt Ltd0 个研究点目标入组 2,500 人待定

概览

阶段
4 期
干预措施
未指定
疾病 / 适应症
Health Condition 1: null- to determine whether periodic therapy programmingreports delivered to study centers can increase the utilization of shock reductionprogramming
发起方
India Medtronic Pvt Ltd
入组人数
2500
状态
已完成
最后更新
4年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
4年前
研究类型
Observational

研究者

入排标准

入选标准

  • 1\. Subject is willing and able to sign and date the PIC and statement regarding use of personal data
  • 2\. Subjects will be screened to ensure they meet all of the inclusion and none of the exclusion criteria.
  • 3\. Both initial generator implants and replacement generators are eligible for enrollment.
  • 4\. Subject has been implanted with a Medtronic market released ICD or CRTD device within the past 30 days
  • 5\. Subject has commercially released RA , RV, and LV leads if applicable

排除标准

  • Subject is enrolled in a concurrent study that has not been approved for concurrent enrollment by the Medtronic Clinical Trial Leader

结局指标

主要结局

未指定

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