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.
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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