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临床试验/NCT03581656
NCT03581656Unknown不适用

ChordArt System Study for the Treatment of Mitral Regurgitation Due to Leaflet Prolapse or Flail

CoreMedic GmbH2 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年3月21日最近更新:
适应症

试验速览

阶段
不适用
入组人数
5
试验地点
2
主要终点
Major adverse events

研究概览

简要总结

The ChordArt System is a novel catheter based technology for mitral chordal replacement that enables controlled implantation of artificial mitral chords to treat mitral regurgitation with a minimally invasive approach. The implant is designed to allow transfemoral antegrade implantation.

详细描述

ChordArt utilizes a minimally invasive catheter based approach by which multiple artificial chordae are precisely positioned into the papillary muscle and then secured to the pathological leaflet.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
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

  • Age ≥ 18 years
  • Mitral Regurgitation due to degenerative mitral leaflet prolapse or flail
  • Left Ventricular Ejection Fraction >20%
  • New York Heart Association functional class II to IV
  • Able and willing to give informed consent and follow protocol procedures.

排除标准

  • Life expectancy <1 year
  • Hemodynamic instability
  • Severe untreated ischemic disease
  • Pulmonary Hypertension
  • Any prior mitral valve surgery or transcatheter mitral valve procedure
  • Stroke or transient ischemic event within 30 days before randomization
  • Patient is pregnant (urine human chorionic gonadotropin (HCG) test result positive), planning to be pregnant or lactating.
  • Renal insufficiency
  • Acute anemia
  • Chronic obstructive pulmonary disease
  • Severe right ventricular dysfunction
  • Hepatic insufficiency
  • Patient is participating in other investigational studies

结局指标

主要结局

Major adverse events

时间窗: At 30 days from implant procedure

The frequency of pre-determined major adverse events

All-cause mortality

时间窗: At 30 days from implant procedure

The frequency of all-cause mortality

次要结局

  • Device Performance(At 30 days)
  • Technical Success(End of Implantation Procedure)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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ChordArt System for Mitral Regurgitation | 临床试验