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临床试验/NL-OMON56551
NL-OMON56551
招募中
不适用

Elective cardioversion of atrial fibrillation at home by advanced practice providers; A feasibility study in Dutch emergency medical service. - ELECTRA-1

Jeroen Bosch ziekenhuis0 个研究点目标入组 25 人待定

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
atrial fibrilation
发起方
Jeroen Bosch ziekenhuis
入组人数
25
状态
招募中
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Interventional

研究者

发起方
Jeroen Bosch ziekenhuis

入排标准

入选标准

  • 1\. 1\. Signed informed consent 2\. Age 18 \-75 year subjects, able to understand
  • the provided information and sign an informed consent 3\. Need for direct
  • current electrical cardioversion (DC\-ECV) for correction of recurrent
  • symptomatic AF (according to the guidelines of the American College of
  • Cardiology/American Heart Association/European Society of Cardiology
  • (ACC/AHA/ESC)). 4\. Weight more than 50 kilograms 5\. Successful hospital DC\-ECV
  • for a previous episode of AF performed under propofol sedation 6\. Target range
  • of international normalized ratio (INR) above 2\.0, when on vitamin K
  • antagonists, or use of novel oral anticoagulant, stable for 3 weeks 7\. ASA 2 8\.
  • BMI \< 35 kg/m2

排除标准

  • 1\. Patients over 75 years old and younger than 18 years 2\. Patients wearing
  • pacemaker or implantable cardioverter\-defibrillator. 3\. Patients with
  • (cardiovascular): \* sick sinus syndrome, ventricular pre\-excitation, Brugada
  • syndrome or bundle branch block \* severe ischemic or valvular heart disease \*
  • known second or third degree atrioventricular block normal sinus rhythm \* heart
  • failure NYHA III or IV, known LVEF \< 35%, or cor pulmonale \* transient and
  • reversible cause of AF, e.g. in setting of fever and hyperthyroidism 4\.
  • Patients with severe co\-morbidities: a. liver disease b. kidney impairment
  • (eGFR \<\= 30 according to formula MDRD) c. pulmonary dysfunction (FEV1 /VC \<75%
  • gold classification) d. active malignancy e. connective tissue disease f.

结局指标

主要结局

未指定

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