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临床试验/NCT03941275
NCT03941275已完成不适用

SelectSecure 3830 Lead Imaging

Medtronic Cardiac Rhythm and Heart Failure4 个研究点 分布在 1 个国家目标入组 51 人开始时间: 2019年5月24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
入组人数
51
试验地点
4
主要终点
Collect high quality shoulder and intracardiac bi-plane fluoroscopic cine images of the SelectSecure 3830 pacing lead.

研究概览

简要总结

This study is designed to collect high-quality shoulder and intracardiac bi-plane fluoroscopic images during two standard arm motions on patients implanted with a market released SelectSecure 3830 lead for the purposes of developing a fracture reliability model.

研究设计

研究类型
Observational
观察模型
Other
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

  • Patients who are at least 18 years of age
  • Patient has a pacing, ICD or CRT system incorporating at least one SelectSecure 3830 lead in the right atrium or right ventricle
  • Patients able and willing to attend imaging session
  • Patients able and willing to give informed consent
  • Pacing capture threshold and pacing impedance of the lead are within normal range at the time of enrollment
  • Patient must be able to accomplish arm flexion and adduction past 90 degrees

排除标准

  • Subjects who require a legally authorized representative to obtain consent
  • Subjects with exclusion criteria required by local law (e.g. age, breastfeeding)
  • Pregnant women, or women of child bearing potential and who are not on a reliable form of birth control
  • Subjects that were implanted with a pacing, ICD, CRT device and/or cardiac leads less than three months ago

结局指标

主要结局

Collect high quality shoulder and intracardiac bi-plane fluoroscopic cine images of the SelectSecure 3830 pacing lead.

时间窗: approximately 30 minutes

Fluoroscopic cine images will be collected in conjunction with a specialized calibration object. When imaging data is processed and analyzed it will characterize the time-varying lead shape changes.

次要结局

  • Acquire accelerometer-based motion data(approximately 30 minutes)

研究者

发起方
Medtronic Cardiac Rhythm and Heart Failure
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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