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临床试验/NL-OMON26814
NL-OMON26814招募中不适用

INGENIO MRI/ FINELINE II ImageReadyTM pacing system data collection in patients undergoing Magnetic Resonance Imaging.

Giovanni RacitiClinical Trial ManagerPhone: +39 02 26983213E-mail: Giovanni.Raciti@bsci.com0 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
招募中
发起方
入组人数
20

研究概览

简要总结

/A

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Age 18 or above, or above legal age and willing and capable of giving informed consent specific to national law;
  • 2. Patients already implanted with ImageReady™ MR Conditional Pacing System, single or dual chamber, including INGENIO MRI or ADVANTIO MRI pulse generators with FINELINE II Sterox or FINELINE II Sterox EZ endocardial lead(s), according to standard medical guidelines for pacemaker implantation;

排除标准

  • 1. Patients implanted with pulse generator location outside of left or right pectoral regions;
  • 2. Patients implanted with other cardiac-related implanted devices or accessories other than the ImageReadyTM MR Conditional Pacing System;

研究者

发起方
Giovanni RacitiClinical Trial ManagerPhone: +39 02 26983213E-mail: Giovanni.Raciti@bsci.com

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