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临床试验/NCT00170261
NCT00170261已完成4 期

Early Loop-Recorder in Suspected Arrhythmogenic Syncope

Medtronic Cardiac Rhythm and Heart Failure6 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2002年4月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
100
试验地点
6
主要终点
Cost of diagnostics per patient until final cardiac diagnosis has been made

研究概览

简要总结

This is a prospective, controlled, opened randomized study to evaluate the cost benefit of a primary implantation of a loop recorder versus the conventional diagnostic cascade for syncope most likely due to cardiac arrhythmia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

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

  • Two or more episodes of syncope (most likely due to cardiac arrhythmia) of uncertain etiology within the last 12 months or more than one syncope and two presyncopes

排除标准

  • Indication for the implantation of a pacemaker
  • Indication for the implantation of an implantable cardioverter defibrillator
  • Cardiac diseases which need intervention (KHK, aortic stenosis, mitral stenosis, left ventricular [LV] outflow stenosis, decompensated heart failure)
  • Contraindication for a diagnostic procedure requested by the study protocol
  • Enrollment in another study
  • Circumstances or comorbidities which do not allow enrollment

结局指标

主要结局

Cost of diagnostics per patient until final cardiac diagnosis has been made

次要结局

  • Cost of diagnostics until final diagnosis has been made
  • Rate of correct cardiac diagnoses
  • Comparison of time needed to make a diagnosis
  • Comparison of pre-syncopes and syncopes occuring in both groups after enrollment

研究者

发起方
Medtronic Cardiac Rhythm and Heart Failure
申办方类型
Industry

研究点 (6)

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