跳至主要内容
临床试验/DRKS00015681
DRKS00015681招募中不适用

Sorin Universal REgistry on Aortic Valve Replacement - SURE-AVR

Sorin Group Italia S.r.l.0 个研究点目标入组 5,000 人开始时间: 2018年10月4日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
5,000

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
one 至 one(—)
性别
All

入选标准

  • All patients having received a Sorin Group aortic valve device in accordance with the IFU can be included in the registry. Other than the indication and the contra-indications specified in each IFU, there are no specific inclusion and exclusion criteria since this registry has the aim to include all patients following real life”/standard of care practices at participating centers. All patients must provide written or oral informed consent to participate in the registry following the local regulations.

排除标准

  • Any contra indication(s) for valve Implantation.

研究者

发起方
Sorin Group Italia S.r.l.

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