跳至主要内容
临床试验/NCT03891329
NCT03891329已完成不适用

BIO|MASTER.Cor Family Study

Biotronik SE & Co. KG13 个研究点 分布在 7 个国家目标入组 130 人开始时间: 2019年4月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
试验地点
13
主要终点
Cor Family-related Serious Adverse Device Effect (SADE)-Free Rate Until 3-month Follow-up

研究概览

简要总结

Post-Market Clinical Follow-up of the new Cor Family ICDs/CRT-Ds (Acticor, Rivacor) and the new Plexa ProMRI S DX right ventricular lead to provide post-market data and supporting evidence for the clinical safety and performance of the devices.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Standard indication for ICD or CRT-D therapy according to clinical guidelines
  • Planned for de novo implantation of an ICD/CRT-D, or upgrade/exchange from existing ICD/CRT-D or pacemaker implant
  • Able to understand the nature of study and to provide written informed consent
  • Willing and able to perform all follow-up visits at the study site
  • Willing and able to use the CardioMessenger and accepts the BIOTRONIK Home Monitoring concept

排除标准

  • Contraindication to ICD and CRT-D therapy
  • Planned for implantation of a CRT-DX system
  • For VR-T DX devices: permanent atrial tachyarrhythmia
  • For VR-T DX devices: patients requiring atrial pacing
  • Less than 18 years old
  • Pregnant or breast feeding
  • Participating in another interventional clinical investigation
  • Life-expectancy is less than 12 months
  • Cardiac surgical procedure planned within 12 months after implantation (including interventional procedures like ablation, valve replacement, heart transplant etc.). Procedures to occur during or prior to implantation are not exclusionary

结局指标

主要结局

Cor Family-related Serious Adverse Device Effect (SADE)-Free Rate Until 3-month Follow-up

时间窗: 3 months

Serious Adverse Device Effect (SADE)-free rate possibly or securely related to the Cor Family Internal Cardioverter Defibrillators (ICDs) / Cardiac Resynchronisation Therapy-Defibrillators (CRT-Ds) until 3-month follow-up

次要结局

  • Kaplan-Meier Estimate for the Cor Family Related SADE-free Rate(3 months, 12 months)
  • Number of Handling-Assessments of the Automatic LV VectorOpt Test (CRT-devices Only) by the Investigator(3 months)
  • Number of Handling-Assessments for the Overall Handling of the CRT AutoAdapt Feature (CRT-devices Only) by the Investigator(3 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (13)

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