NL-OMON28451已完成不适用
INGENIO 2 /INGEVITY MRI device family data collection in patients undergoing Magnetic Resonance Imaging
study sponsored by:Guidant Europe SA / NV,a Boston Scientific CompanyClinical CRM Department Green SquareLambroekstraat 5D 1831 Diegem, Belgium0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Age 18 or above, or above legal age and willing and capable of giving informed consent specific to national law
- •Patients already implanted with ImageReady™ MR Conditional Pacing System, according to standard medical guidelines for pacemaker implantation.
- •Willing and capable of participation to the procedures indicated in the protocol.
排除标准
- •Patients implanted with other cardiac-related implanted devices or accessories other than the ImageReadyTM MR Conditional Pacing System
- •Low life expectancy (< 1 year)
- •Severe comorbidities that, according to clinical judgment, pose patient at risk to undergo MRI
研究者
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招募中
不适用
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