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)).
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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