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临床试验/NL-OMON43812
NL-OMON43812已完成不适用

Aortic Stenosis * Identification of high-risk valve pathology using STRESS physiology (AoS-STRESS) - AoS-STRESS

Catharina-ziekenhuis0 个研究点目标入组 50 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
50

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

  • -Age * 18 years.
  • -Undergoing TAVI or balloon valvuloplasty for standard clinical indications/undergoing coronary catheterization and have had an echo with a moderate aortic stenosis in the last 3 months
  • -Ability to understand and the willingness to sign a written informed consent.

排除标准

  • -Unrevascularized and severe coronary artery disease (for example a 90% diameter stenosis or FFR<0.7 in the proximal left anterior descending artery) that in the opinion of the primary TAVI/BAV operator would produce significant ischemia during dobutamine infusion.
  • -Significant aortic regurgitation, mitral valve disease, tricuspid regurgitation, or intracardiac shunt that would invalidate thermodilution cardiac output or the interpretation of transvalvular flow across the aortic valve.
  • -Co-existing hypertrophic cardiomyopathy.
  • -Atrial fibrillation or tachycardia with rapid ventricular response, a history of significant ventricular tachycardia or fibrillation, or an implanted cardiac defibrillator whose treatment thresholds would be reached during dobutamine infusion.
  • -Known hypersensitive response to dobutamine.
  • -Recent (within 3 weeks prior to cardiac catheterization) ST-segment elevation myocardial infarction (STEMI) in any arterial distribution.

研究者

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