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临床试验/NCT04253184
NCT04253184已完成不适用

Micra AV Transcatheter Pacing System Post-Approval Registry

Medtronic135 个研究点 分布在 3 个国家目标入组 802 人开始时间: 2020年2月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Medtronic
入组人数
802
试验地点
135
主要终点
Rate of pacemaker syndrome

研究概览

简要总结

Medtronic is sponsoring the Micra AV Registry using the Micra AV system for continued surveillance of chronic atrioventricular synchronous pacing as intended, through the collection of data based on routine clinical care practice, following commercial release.

The Micra AV Registry is conducted within Medtronic's Product Surveillance Registry (PSR) platform.

详细描述

The Micra AV Registry is a global, prospective, observational, multi-site registry. Patients enrolled in the Micra AV Registry will be prospectively followed for a minimum of 3 years post-implant or until registry closure, patient death, patient exit from the registry (i.e., withdrawal of consent).

Enrolled patients will have scheduled follow-up visits at least annually or as prompted by reportable adverse events; however, all Micra AV system follow-up patient visits are to be reported. Therefore, if more frequent scheduled visits occur per a provider's routine clinical care practice, those visits are reported. The total estimated registry duration is 4.5 years

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
  • Patient is intended to receive or be treated with a Micra AV Transcatheter Pacing System and must be enrolled prior to the implant procedure

排除标准

  • Patient who is, or is expected to be inaccessible for follow-up
  • Patient with exclusion criteria required by local law
  • Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results

结局指标

主要结局

Rate of pacemaker syndrome

时间窗: After 3 years of Follow Up

To characterize the rate of pacemaker syndrome resulting in a system revision at 3-years post-implant.

次要结局

  • Acute complication rate(After 30 days of Follow Up)
  • Long-term complication rate(After 3 years of Follow up)

研究者

发起方
Medtronic
申办方类型
Industry
责任方
Sponsor

研究点 (135)

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