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临床试验/NCT04200014
NCT04200014Unknown不适用

Bradycardia High Risk Patient Identification After Syncope With Loop Recorder an Observational Study in Nancy University Hospital

Central Hospital, Nancy, France1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2019年12月9日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
250
试验地点
1
主要终点
significant bradycardia whitch result with an Indication of pacemaker implantation

研究概览

简要总结

Syncope is a common symptom that may be related to a conductive disorder. If no bradycardia is authenticated, it is often necessary to implant an implantable loop recorder.

In somes cases, implantable loop recorder records cardiac conductive disorders. In this study, we want to try to identify a group of patients for whom we could immediately implant a pacemaker without prior implantation of an implantable loop recorder given the high probability of implantation of a pacemaker after interrogation of the implantable loop recorder. It would be interesting for the reduction of interventions for the patients and for the economic aspect of the healthcare system

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • All patients who have benefited from an Implantable Loop recorder in the Nancy's Teaching Hospital

排除标准

  • No Exclusion Criteria

结局指标

主要结局

significant bradycardia whitch result with an Indication of pacemaker implantation

时间窗: At the moment of enregistrement of a significative arrhythmia or at the end of the 3 years of follow up

2° and 3° AV block, sinus node dysfunction with pause \> 8 sec or \> 3sec with concomitant symptoms, sick sinus syndrom

次要结局

  • Patient group without benefit of implantation of the Implantable Loop Recorder(At the end of the 3 years of follow-up)

研究者

发起方
Central Hospital, Nancy, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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