PACTR202201680255620已完成4 期
Efficacy of intraoperative low dose intravenous amiodarone in pharmacologic cardioversion in patients with preoperative atrial fibrillation presenting for mitral valve replacement surgery Randomized control trial
未提供0 个研究点目标入组 90 人开始时间: 2022年1月24日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 90
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- All
入选标准
- •· All elective isolated cases undergoing mitral valve replacement with a preoperative atrial fibrillation rhythm > 100/min as evidenced by ECG.
- •· ASA physical status 2-5
- •· Sex (males and females)
- •· Age 18-70 years.
排除标准
- •· Patients are refusing to participate in the study.
- •· Below 18 or above 60 years.
- •· Emergency and urgent patients.
- •· Patients are undergoing combined valve or CABG surgery.
- •· Patients with previous PCI.
- •· Patients with rhythm defects evidenced by ECG.
- •· Patient on amiodarone or other rhythm modifying drugs, e.g., Digoxin, Beta Blockers, CCBs, etc.
- •· Patients with preoperative lung conditions or O2 saturation below 90%.
- •· Patients with preoperative abnormal hepatic profiles identified by double average values of ALT/AST or bilirubin or hypoalbuminemia
- •· Patients with preoperative renal impairment identified by serum creatinine more than 1.7 mg/dL
- •· Abnormal thyroid profile or any history suggestive of thyroid diseases.
- •· Diabetic patients, as the study, include Dextrose 5% based medication.
研究者
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