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临床试验/NCT03526302
NCT03526302已完成不适用

Register About Change of hsTROPoninT After Implantation of a Subcutaneous Implantable Cardioverter-Defibrillator

Deutsches Herzzentrum Muenchen1 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2018年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
43
试验地点
1
主要终点
High sensitive TroponinT

研究概览

简要总结

Serum Troponin levels pre- and postoperatively will be compared in patients receiving an entirely subcutaneous cardioverter-defibrillator.

详细描述

To analyze the periprocedural myocardial damage the pre- and postoperative assessment of serum levels of high sensitive TroponinT (hsTnT) is done. The main objectives of the TROPIC register are to evaluate the level of high sensitive TroponinT before and after S-ICD device implantation and to compare these changes in TroponinT-levels with those after standard transvenous ICD-implantation.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Indication for the implantation of an entirely subcutaneous cardioverter-defibrillator

排除标准

  • 未提供

结局指标

主要结局

High sensitive TroponinT

时间窗: 24 hours

Difference between pre- and postoperative high sensitive TroponinT serum levels

次要结局

未报告次要终点

研究者

发起方
Deutsches Herzzentrum Muenchen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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