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临床试验/NCT01236469
NCT01236469已完成不适用

CryoValve® SG Aortic Human Heart Valve Combination Retrospective/Prospective, Multi-Center, Cohort Study

CryoLife, Inc.9 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2010年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
9
主要终点
Hemodynamic Performance

研究概览

简要总结

The purpose of this study is to assess the probable benefit of CryoValve SG Aortic Human Heart Valve used in pediatric patients as an aortic valve replacement.

详细描述

The CryoValve SG aortic human heart valve is recovered from deceased human donors, treated with the SynerGraft® (SG) process,which is designed to reduce the donor cells present on the graft. The valve is then cryopreserved for storage until use. Removing cells from the heart valve has been shown to reduce a component of the immune response after implant compared to a standard allograft valve. However, it is not known how this affects the long-term durability of the valve.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
6 Years 至 27 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients implanted with a CryoValve SGAV as an aortic valve replacement.
  • Patients who were ≤ 21 years of age at the time of implant.

排除标准

  • Patients in whom the CryoValve SGAV was used as a patch or a non-valved conduit.
  • Patients implanted with a CryoValve SGAV as a pulmonary valve replacement.
  • Patients that were ≥ 22 years of age at the time of implant.

结局指标

主要结局

Hemodynamic Performance

时间窗: From Implant until Study Enrollment (on average, 7 years)

Peak Aortic Gradient (or Peak Velocity), Mean Aortic Gradient, Aortic Insufficiency, Effective Orifice Area

Number of Adverse Events as a Measure of Safety

时间窗: From Implant until Study Enrollment (on average, 7 years)

Safety parameters will follow the guidelines for reporting morbidity and mortality after cardiac valvular operations as established by The American Association for Thoracic Surgery and The Society of Thoracic Surgeons. Evaluation of the following adverse events: * Mortality (all cause and valve-related) * Reoperation/reintervention * Explant * Endocarditis (all and valvular) * Thrombosis * Thromboembolism * Non-structural dysfunction * Perivalvular leak (all and major) * Bleeding (all and major) * Hemolysis * Calcification * Conduit failure

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (9)

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