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临床试验/EUCTR2013-005533-20-BE
EUCTR2013-005533-20-BE进行中(未招募)1 期

Volatile anesthetics to reduce mortality in cardiac surgery. A multicentre randomized controlled study. - Volatile anesthetics to reduce mortality in cardiac surgery.

Ghent University Hospital0 个研究点目标入组 5,200 人开始时间: 2016年1月22日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
5,200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • -age >18 years
  • -written informed consent
  • -scheduled procedures
  • -planned isolated CABG (multiple bypass are allowed; planned combined intervention such as CABG plus valve surgery are not allowed)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10600
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -pregnancy
  • -planned valve surgery or surgery on the aorta
  • -planned locoregional anesthesia without general anesthesia
  • -unstable or ongoing angina
  • -recent (< 1 month) or ongoing acute myocardial infarction
  • -use of sulfonylurea, theophylline or allopurinol
  • -previous unusual response to an anesthetic agent
  • -inclusion in other randomised controlled studies in the previous 30 days
  • -any general anesthesia performed in the previous 30 days
  • -emergency operation (not scheduled)
  • -kidney or liver transplant in medical history
  • -liver cirrhosis (Child B or C)
  • -patients with absolute contraindications to anesthetic agents as per summary of product characteristics

研究者

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