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临床试验/NCT02981004
NCT02981004已完成不适用

PAR I - Prothesis-to-Annulus Relation (PAR) as Predictor of Hemodynamic Outcome in Aortic Valve Replacement

Abbott Medical Devices7 个研究点 分布在 1 个国家目标入组 304 人开始时间: 2012年10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
304
试验地点
7
主要终点
recording of hemodynamic outcome of a aortic valve in mutual dependence of anatomical facts on the basis of echocardiographic parameter

研究概览

简要总结

The Prosthesis-to-Annulus Relation I (PAR I) trial is a German multicenter study assessing the relation between the prosthetic GOA and the area of LVOT as potentially new parameter for the prediction of hemodynamic outcome. The results may possibly guide future valve size selection an may allow prediction of functionally relevant PPM (Patient-Prosthesis-Mismatch)

详细描述

Great debates revolve around the hemodynamic performance of prosthetic tissue valves. It is influenced by the design and the specific sizing strategy. Design determines the actual geometric orifice area (GOA), sizing strategy the actual size of the selected valve. Currently, hemodynamic performance is generally assessed by determining the effective orifice area (EOA, derived from the continuity equation by relating flow velocities and LVOT area). The question whether a prosthesis patient mismatch (PPM) is present is then addressed by relating EOA to body surface area (EOAi). However, this relation may not be reasonable because EOAi relates flow velocity twice to patient-specific anatomic parameters (LVOT area and body surface area) . Considering this potential methodological flaw, debate and confusion regarding PPM is easily understood, despite the fact that, intuitively leaving a gradient behind after aortic valve replacement cannot be irrelevant. Thus a reliable and comparable method to determine the presence of PPM is needed. In PAR I Trial the relation between true prothetic GOA and LVOT area will be assesses as a potentially new parameter for prediction of hemodynamic outcome, to possibly guide future valve size selection (inclusive valve-in-valve) and to allow the detection of functionally relevant PPM. In the trial it will be assessed how anatomic dimensions of patients and implanted valves relate to each other and whether they allow the prediction of hemodynamic outcome.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

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

  • 1.Patient has an indication for primary, isolated aortic valve implantation
  • Patient is above 18 Years old
  • Patient has signed patient informed consent
  • foreseen implantation of an Epic, Epic supra or Trifecta valve
  • Patient has sinus rhythm

排除标准

  • Patient is younger than 18 years
  • Patient has active endocarditis
  • Patient is not able or does not want to participate on follow-up
  • Patient is pregnant or nursing
  • Surgical widening of outflow tract is planned
  • Left ventricular ejection fraction is smaller than 50%
  • Patient has a mitral valve or tricuspid valve insufficiency or stenosis bigger or equal Grade II

结局指标

主要结局

recording of hemodynamic outcome of a aortic valve in mutual dependence of anatomical facts on the basis of echocardiographic parameter

时间窗: postprocedure before discharge (less than 30 days after implant)

Echocardiographic evaluation of the anatomical facts e.g. Left ventricular outflow area

次要结局

  • Mortality 30 days after implant(30 days)
  • Morbidity 30 days after implant(30 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (7)

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