JPRN-jRCT1022230003招募中Unknown
A multicenter prospective randomized study to evaluate the delivery timing safety and efficacy of AntiTachycardia Pacing - BIO|ATP
Ando Kenji0 个研究点目标入组 398 人开始时间: 2023年5月15日最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 398
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
- 年龄范围
- >= 18age old 至 ot applicable（—）
- 性别
- All
入选标准
- •Patient has an indication for ICD according to the JCS / JHRS 2021 Guideline Focused Update on Non-Pharmacotherapy of Cardiac Arrhythmias
- •- Patient is either planned for de novo ICD implantation or is already implanted with an investigational ICD for 10 days or less
- •- Patient can be treated with ATP therapy for both VT and VF zone
- •- Patient is willing and able to use the CardioMessenger and accepts the Home Monitoring concept
- •- Patient is willing to visit the hospital in accordance with physicians instruction
- •- Patient is able to understand the nature of the study and to provide written informed consent
排除标准
- •- Patient planned for implantation with or already implanted with CRT-D device
- •- A patient who is confirmed to have received ICD therapy
- •- A patient who is diagnosed as Idiopathic VF (e.g. Brugada syndrome, Long QT Syndrome, other IVF)
- •- Age < 18 years
- •- A patient who has impaired mental status
- •- Life expectancy less than 18 months
- •- Participation in another interventional clinical investigation
- •- Pregnant or breastfeeding
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