Investigating Significant ICD Heart Therapies Registry Study (INSIGHTS ICD Registry)

Medtronic Cardiac Rhythm and Heart Failure0 个研究点目标入组 1,326 人开始时间: 2004年2月最近更新: 2007年12月28日

适应症

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 1,326

研究概览研究设计入排标准研究者记录与标识符相似试验

研究概览

简要总结

The purpose of the Registry is to collect data on how Implantable Cardioverter Defibrillator (ICD) therapies and medications are being used by physicians to treat ventricular arrhythmias in order to better understand how to improve the clinical care of patients and effectiveness of ICD therapies.

研究设计

研究类型: Observational
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: 否

入选标准

•Patients 18 years of age or older.
•Patients or legal guardians who are willing and able to sign a Permission for Access to and Use of Health Information in a Registry Form and, if required by an Institution's IRB, an Informed Consent.
•New or replacement implants of Medtronic market released single, dual or triple chamber ICDs including: GEM VR, GEM DR, GEM III AT, Marquis VR, Marquis DR, Maximo DR, Maximo VR, InSync ICD, InSync Marquis ICD and InSync II Marquis ICD.

排除标准

•Patients enrolled in a device study which effects programming and or treatment.

研究者

发起方

Medtronic Cardiac Rhythm and Heart Failure

申办方类型

Industry

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