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临床试验/ACTRN12607000436471
ACTRN12607000436471
招募中
不适用

sing Cerebral oximetry (INVOS 5100) during cardiopulmonary bypass in patients requiring elective isolated coronary artery bypass graft surgery to improve neuropsychological outcomes or composite clincal outcomes (composite endpoint based on the presence of 30-day mortality or a major morbidity (permanent stroke, renal dysfunction or failure, cardiac surgery reoperation, prolonged ventilation, deep sternal wound infection)).

Flinders Medical Centre0 个研究点目标入组 300 人2007年8月29日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
未指定
发起方
Flinders Medical Centre
入组人数
300
状态
招募中
最后更新
6年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2007年8月29日
结束日期
待定
最后更新
6年前
研究类型
Interventional
性别
All

研究者

入排标准

入选标准

  • The patient sample: will consist of participants of both gender, requiring elective isolated coronary artery bypass graft surgery at Flinders Medical Centre;
  • The patient is willing to participate and has signed a consent form.

排除标准

  • English not first language;
  • Previous cerebrovascular disease including CVA, RIND, or TIA anytime prior to planned surgery;
  • Emergency and urgent coronary artery surgery
  • Previous open heart surgery
  • History of neurological disease/insult

结局指标

主要结局

未指定

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