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临床试验/NCT01522911
NCT01522911Unknown不适用

Interventional Study to Investigate the Effects of Percutaneous Closure of the Left Atrial Appendage on Atrial and Brain Natriuretic Peptide Secretion

University of Leipzig0 个研究点目标入组 50 人开始时间: 2010年5月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
50
主要终点
Change from Baseline Plasma ANP and BNP levels after transcatheter closure of the left atrial appendage.

研究概览

简要总结

To date there are no data suggesting substantial effects of hormonal interaction after percutaneous closure of the left atrial appendage (LAA). Our hypothesis is that by excluding the LAA from blood flow physiologic stimuli for ANP and BNP produce may be impaired and consecutive release of the hormones may be reduced. Here, we present our experience of ANP and BNP secretion in the early postprocedural period after transcatheter closure of the LAA.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • non-valvular atrial fibrillation
  • increased risk for thromboembolic complications (a minimum CHADS2Score of at least 2)

排除标准

  • Valvular-atrial fibrillation
  • Low risk for thromboembolic complications CHADS-2-Score < 2

结局指标

主要结局

Change from Baseline Plasma ANP and BNP levels after transcatheter closure of the left atrial appendage.

时间窗: participants will be followed for the duration of hospital stay, an expected average of 48 hours

Venous blood samples are taken before the procedure, immediately after implantation of the LAA closure device and on the first morning after the procedure. The blood is drawn into plastic tubes containing aprotinin and ethylenediaminetetraacetic acid disodium and is promptly centrifuged. The plasma obtained is stored at -20°C until assayed. The plasma BNP and ANP concentrations are then determined with a commercially available enzyme immunoassay kit (ELISA Kit for Brain Natriuretic Peptide, Uscn Life Science Inc., Missouri City, USA and ANP ELISA Kit, Hölzel Diagnostika, Köln, Germany).

次要结局

未报告次要终点

研究者

发起方
University of Leipzig
申办方类型
Other
责任方
Principal Investigator
主要研究者

Nicolas Majunke

senior physician

University of Leipzig

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