跳至主要内容
临床试验/KCT0002960
KCT0002960招募中未知

ong Term Evaluation and Management of Atrial Fibrillation in Pacemaker Patients (AF-pacemaker Tx study)

Yonsei University Health System, Severance Hospital0 个研究点目标入组 135 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
135

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 90(Year)(—)
性别
All

入选标准

  • 1. Patients who diveloped drug-refractory atrial fibrillation/flutter/tachycardia after pacemaker implantation among AF-pacemaker study (ClinicalTrials.gov Identifier: NCT03303872).
  • 2. Age: 18-80 years
  • 3. Patients eligible for the indications for permanent pacemaker implantation in accordance with 2016 revised Korean indication guideline on cardiac pacemaker implantation
  • 4. Estimated percentage of atrial pacing >40% under sinus rhythm (LR=60bpm, close hysteresis and rest rate)
  • 5. Estimated percentage of ventricular pacing >40% under sinus rhythm (LR=40bpm, DDD pacing, close hysteresis and rest rate)
  • 6. Patients who are willing to sign the informed consent.
  • 7. Patients who are willing to receive the implantation and post-operative follow-up.

排除标准

  • 1. Persistent or permanent AF
  • 2. Severe hepatic and renal insufficiency (AST or ALT = three times of normal upper limit; SCr > 3.5 mg/dl or Ccr < 30ml/min)
  • 3. Thyroid gland dysfunction
  • 4. Pregnancy
  • 5. Malignant tumor
  • 6. Severe organic heart disease (such as moderate to severe mitral regurgitation, severe valvular regurgitation and stenosis, dilated cardiomyopathy, hypertrophic cardiomyopathy, severe heart valve disease)
  • 7. Life expectancy < 12 months
  • 8. Patients unable or unwilling to cooperate in the study procedures.

研究者

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