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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 人开始时间: 2007年8月29日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
300

研究概览

简要总结

暂无简介。

研究设计

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

入排标准

年龄范围
18 Years 至 ot stated(—)
性别
All

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

研究者

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