跳至主要内容
临床试验/NL-OMON43837
NL-OMON43837已完成不适用

International long-term follow-up study of patients implanted with a PORTICO* valve - Portico I

St. Jude Medical0 个研究点目标入组 30 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
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Patient has signed the Patient Informed Consent prior to participating in the clinical investigation.
  • 2. Patient has been referred for a Portico Valve implant as per Heart Team decision.
  • 3. Patient has senile degenerative aortic valve stenosis confirmed by echocardiographically derived criteria
  • 4. Patient has a life expectancy of more than (>) 12 months.

排除标准

  • 1. Any case in which the Portico Valve would not be indicated for the patient as per current IFU (i.e. any *off-label* use).
  • 2. Patient has any other aortic valve than tricuspid one.
  • 3. Patient has a prosthetic valve or ring in the aortic position.
  • 4. Patient needs a concomitant structural heart procedure.
  • 5. Patient is unwilling or unable to comply with all clinical investigation-required follow-up evaluations.
  • 6. Patient is pregnant

研究者

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