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临床试验/NCT03750058
NCT03750058已完成不适用

AXONE -Acute : Acute Assessment of a Micro Multipolar Lead for Enhanced Cardiac Resynchronisation Therapy

University Hospital, Rouen4 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年8月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
4
主要终点
LV Multizone pacing success rate

研究概览

简要总结

Pilot study to evaluate the performance of a lead below 2 French with specific distal shape to deliver efficient LV pacing

研究设计

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

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

  • Male or female patient aged ≥18 years old.
  • Patient presenting a CRT-P or CRT-D indication according to the latest ESC guidelines .
  • Primary implant of a CRT device (including upgrade from a single or dual-chamber pacemaker or ICD).
  • Signed and dated informed consent.
  • Patient affiliated with, or beneficiary of a social security category.

排除标准

  • Class IV of NYHA (ambulatory or not).
  • Allergy to contrast media used for imaging during cardiac catheterization.
  • Severe Renal Failure (clearance of creatinine < 30ml/mn/m²).
  • Previous failure catheterization of the coronary sinus, or previous failure of left ventricular lead implantation.
  • Already included in another clinical study involving intra-cardiac active implantable device, or participation to any other clinical trial in the last 2 weeks.
  • Person deprived of liberty by administrative or judicial decision or placed under judicial protection (guardianship or supervision).
  • Known pregnancy, breastfeeding women or in childbearing age without an adequate contraceptive method (failure rate < 1%).

研究组 & 干预措施

Implant test procedure

Experimental

Implant test procedure with new LV quadripolar lead before a standard implantation for Cardiac resynchronisation therapy

干预措施: Implant test procedure (Device)

结局指标

主要结局

LV Multizone pacing success rate

时间窗: 20 min

Percent of patients where the placement of the AXONE lead provides two distant LV pacing vectors matching Pacing Threshold ≤ 3.5V/0.5ms

LV pacing success rate

时间窗: 20 min

Percent of patients where the placement of the AXONE lead allows at least one LV pacing vector matching Pacing Threshold ≤ 3.5V/0.5ms

次要结局

  • Implant testing Procedure-related Adverse Events procedure.(1 month post testing)
  • Electrical performance of device (1)(20 min)
  • Satisfaction of implanter(20 min)
  • Electrical performance of device (2)(20 min)
  • Lead Implant Efficiency(20 min)

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (4)

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