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临床试验/NCT02697448
NCT02697448已完成不适用

Comparison of Propofol and Sevoflurane as a Primary Anesthetic for Cardiac Ablation of Atrial Fibrillation.

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2016年6月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
135
试验地点
1
主要终点
Procedure Duration

研究概览

简要总结

Comparison of propofol and sevoflurane as a primary anesthetic for cardiac ablation of atrial fibrillation

详细描述

A side effect of some volatile anesthetics, such as isoflurane and desflurane, is enhanced automaticity, accounting for secondary atrial pacemakers. Volatile anesthetics also have varying effects on the AV node and His-Pukinje system. These agents also prolong the QT interval and, for this reason, volatile anesthetics as a group have at times been avoided for atrial fibrillation ablation due to the fear that they may affect the efficacy of the ablation and increase recurrence. However, sevoflurane does not have the effects shown for other volatile anesthetics cardiac conduction. At this point there has not been a study comparing propofol, a non volatile anesthetic typically used in these cases, to sevoflurane, a volatile anesthetic, to determine if volatile anesthetics should be avoided during these procedures. This study will challenge the existing belief that sevoflurane increases the length of time to ablate atrial fibrillation and also decreases the efficacy of the ablation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • have paroxysmal atrial fibrillation
  • undergoing their first ablation.

排除标准

  • 未提供

研究组 & 干预措施

propofol

Active Comparator

Participants receiving propofol as anesthetic for cardiac ablation.

干预措施: propofol (Drug)

sevoflurane

Active Comparator

Participants receiving sevoflurane as anesthetic for cardiac ablation.

干预措施: sevoflurane (Drug)

结局指标

主要结局

Procedure Duration

时间窗: 1 day

The duration of the procedure in minutes.

Time to Extubation

时间窗: Procedure end time to time of extubation

The time from procedure end to the time the patient is extubated, in minutes. A longer extubation time is a worse outcome.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

George Guldan

Principal Investigator

Medical University of South Carolina

研究点 (1)

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