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临床试验/NCT05543278
NCT05543278
撤回
4 期

Pragmatic Amiodarone Trial to Reduce Postoperative Atrial Fibrillation in Patients Undergoing Cardiac Surgery

Massachusetts General Hospital0 个研究点目标入组 242 人2026年1月1日

概览

阶段
4 期
干预措施
Amiodarone
疾病 / 适应症
Surgery, Cardiac
发起方
Massachusetts General Hospital
入组人数
242
主要终点
Postoperative atrial fibrillation
状态
撤回
最后更新
上个月

概览

简要总结

Postoperative atrial fibrillation is quite common after cardiac surgery with up to 1 in 3 patients experiencing this abnormal heart rhythm. Amiodarone, a medication commonly used to treat atrial fibrillation, has been previously shown to be an effective prophylactic agent at decreasing the occurrence of postoperative atrial fibrillation in patients who underwent coronary artery bypass surgery. However, despite many studies which have demonstrated its effectiveness, it has not been widely used due to the concern of side effects that can occur such as slow heart rate, low blood pressure, and lung toxicity. We have designed a study to test the effectiveness and safety of a short course of postoperative prophylactic amiodarone for patients undergoing non-coronary artery bypass cardiac surgery. We hypothesize that patients who receive the prophylactic amiodarone will have decreased rates of postoperative atrial fibrillation without significantly increased side effects compared to patients who receive the standard postoperative care after non-coronary artery bypass cardiac surgery.

注册库
clinicaltrials.gov
开始日期
2026年1月1日
结束日期
2027年12月1日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Asishana A Osho

Assistant Professor of Surgery

Massachusetts General Hospital

入排标准

入选标准

  • \>= 18 years of age
  • All genders
  • All non-coronary artery bypass cardiac surgery patients
  • Preoperative normal sinus rhythm

排除标准

  • Pre-existing atrial fibrillation or atrial arrhythmias
  • Pre-existing heart block
  • Cardiogenic shock
  • Sick sinus syndrome
  • Marked sinus bradycardia
  • Preoperative amiodarone use
  • Contraindication to amiodarone use
  • PR interval \> 240 ms
  • QTc \> 550 ms
  • 2nd or 3rd degree heart block

研究组 & 干预措施

Amiodarone Arm

In addition to the regular care provided to cardiac surgery patients, those in the Amiodarone Arm will also receive the amiodarone regimen.

干预措施: Amiodarone

Standard of Care Arm

Patients randomized to the Standard of Care Arm will receive the regular care provided to cardiac surgery patients.

结局指标

主要结局

Postoperative atrial fibrillation

时间窗: At least 1 minute duration, occurring before or on postoperative day 7

The occurrence of postoperative atrial fibrillation detected by continuous telemetry, 12-lead electrocardiogram, and/or continuous ambulatory monitoring device through postoperative day 7.

次要结局

  • Stroke(Either in-hospital or within 30 days of procedure)
  • Operative mortality(Either in-hospital or within 30 days of procedure)
  • Postoperative hospital length of stay(Up to 90 days)
  • Readmission(Within 30 days of procedure)
  • Myocardial infarction(Either in-hospital or within 30 days of procedure)
  • Persistence of atrial fibrillation at discharge(Up to 90 days)
  • Transient ischemic attack(Either in-hospital or within 30 days of procedure)
  • Electrical cardioversion(Either in-hospital or within 30 days of procedure)
  • Hemodynamic instability(Either in-hospital or within 30 days of procedure)
  • Initiation of systemic anticoagulation(Either in-hospital or within 30 days of procedure)
  • Symptomatic bradycardia(Either in-hospital or within 30 days of procedure)
  • Number of patients with Amiodarone-related pulmonary toxicity(Either in-hospital or within 30 days of procedure)

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