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临床试验/NCT03965065
NCT03965065Unknown不适用

Comparison of Sutureless Vs. Standard Biological Prostheses for Surgical Aortic Valve Replacement: a Randomised Multicenter Study (Madrid, Spain)

Hospital San Carlos, Madrid2 个研究点 分布在 1 个国家目标入组 350 人开始时间: 2019年6月2日最近更新:
适应症

试验速览

阶段
不适用
入组人数
350
试验地点
2
主要终点
Differences in mid term trans prosthetic gradients

研究概览

简要总结

Multicenter randomised study which aims to compare sutureless Vs. standard bio- prostheses (1:1) among patients undergoing surgical aortic valve replacement in terms of:

  • 6 -month hemodynamic performance.
  • 6 month clinical outcomes including all cause mortality, stroke, myocardial infarction, valve reoperation and major/life threatening bleeding
  • Cost effectiveness

详细描述

This study is aimed to compare clinical and hemodynamic performance of conventional sutured stented bio-prostheses among patients undergoing a surgical aortic valve replacement. The prostheses are not pre specified to be provided by a specific manufacturer, so that any bio prosthesis but transcatheter and scentless aortic valves can be implanted.

The estimated sample size is 350 patients. They will be randomised 1:1 to any of the two arms of the study (standard Vs. sutureless prostheses). The randomisation will be stratified according to the need for a concomitant coronary artery bypass grafting procedure.

Six hospitals in Madrid (Spain) will take part in the study. The period of recruitment will start as soon as June 2019 and is supposed to finish by June 2020 or earlier.

The main outcomes of the study will be measured 6 months after the aortic valve implantation

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients older than 18
  • Pure aortic stenosis or combined aortic stenosis/regurgitation
  • Aortic annulus >18 mm and < 27 mm

排除标准

  • Pregnancy
  • Willing to receive some other prosthesis
  • Concomitant surgery of the ascending aorta or left ventricle outflow tract
  • Endocarditis
  • Emergency
  • Some other concomitant procedure
  • Participation in any other study
  • Previous surgery

结局指标

主要结局

Differences in mid term trans prosthetic gradients

时间窗: 6 month

The differences in mid term trans prosthetic gradients measured by trans thoracic echocardiogram 6 months after the procedure

次要结局

  • Differences in quality if life according to the KCCQ12 questionnaire(6 month)
  • Survival from Combined major adverse cardiovascular event(6 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Manuel Carnero Alcazar

Adult Cardiac Surgeon, MD, PhD

Hospital San Carlos, Madrid

研究点 (2)

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