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临床试验/ACTRN12619001647123
ACTRN12619001647123终止未知

Multi-centre prospective randomised placebo-controlled study to evaluate the role of Intravenous Fentanyl during DC cardioversion for the treatment of acute onset Atrial fibrillation. (DAFF Study – Direct Current Cardioversion, Atrial Fibrillation and Fentanyl use)

Central Coast Local Health District0 个研究点目标入组 128 人开始时间: 2019年11月26日最近更新:
适应症

试验速览

阶段
未知
状态
终止
入组人数
128

研究概览

简要总结

o results available yet for plain english summary

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 100 Years(—)
性别
All

入选标准

  • Adult patients (Age >18 year)
  • Able to provide informed consent to enrol in study
  • Atrial fibrillation deemed clinically appropriate for DC cardioversion using procedural sedation and analgesia.
  • No allergy to Propofol or Fentanyl

排除标准

  • Refusal of consent
  • Allergy to Fentanyl or Propofol
  • Dose of intravenous fentanyl in the preceding 2 hours prior to procedure
  • Atrial fibrillation duration unknown
  • Intercurrent Monoamine Oxidase inhibitor use
  • Severe Impariment of Pulmonary reserve
  • Hepatic failure
  • Renal failure

研究者

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