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临床试验/ISRCTN82728969
ISRCTN82728969已完成不适用

Dual chamber and Atrial Tachyarrhythmias Adverse events Study

Medtronic Inc. (USA)0 个研究点目标入组 360 人开始时间: 2004年1月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
360

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Meet Class I implantation criteria for single chamber implantable cardioverter defibrillator according to guidelines

排除标准

  • 1. Permanent atrial fibrillation
  • 2. Non structural heart disease
  • 3. Patient meets implantation criteria for dual-chamber pacing (symptomatic sinus node disease, all 2nd atrioventricular (AV) block [except asymptomatic Mobitz I] and all 3rd degree AV block)
  • 4. Previous system implanted (ICD or pacemaker)
  • 5. Mechanical right heart valve
  • 6. Medical conditions that would preclude the testing required by the protocol, or limit study participation
  • 7. Unwilling or unable to cooperate or give written informed consent, or the patient is a minor and legal guardians refuse to give informed consent
  • 8. Inaccessible for follow-up at the study centre
  • 9. Biventricular stimulation or re-synchronisation
  • 10. Enrolled or planning to enrol in other clinical trials during the clinical study

研究者

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