跳至主要内容
临床试验/jRCTs052210081
jRCTs052210081招募中不适用

Multi Point Pacing and Continuous Atrioventricular Conduction OPtimization of Cardiac Resynchronization Therapy (PPAP-CRT)

未提供0 个研究点目标入组 50 人开始时间: 2022年3月28日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
50
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • A patient who has never received CRT
  • A patient who is eligible for CRT according to the guideline of The Japanese Circulation Society(JCS) and scheduled for implantation of CRT-D
  • A patient with a fixed residence who can follow the scheduled follow-up
  • A patient who has signed and dated the informed consent

排除标准

  • A patient who is suffering from AV block (excluding atrial conduction time 250 ms or more)
  • A patient who is suffering from chronic atrial fibrillation
  • A patient who underwent tricuspid valve surgery or has tricuspid cardiac surgery planned
  • A patients who has a life expectancy of less than 2 years with a non-cardiac cause
  • A patient who is pregnant, breastfeeding or may become pregnant
  • A patient who is less than 20 years of age at the time of consent
  • A patient who is already included or will enroll in another interventional study during this study
  • A patient who is judged by the Principal Investigator (PI) or the Sub-Investigator (SI) as ineligible for participation in this study due to another reason

结局指标

主要结局

-

CRT responder rate at 6 months after CRT-D implantation

次要结局

  • Change in serum brain natriuretic peptide
  • Change in cardiac function
  • Change in echocardiogram

研究者

发起方
未提供

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