ACTRN12618001320246已完成未知
OPtimisation of Perioperative Cardiovascular Management to Improve Surgical outcomE II trial (Optimise II) - biomarker sub-study for Australian sites
St Vincent's Hospital Melbourne0 个研究点目标入组 103 人开始时间: 2018年8月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 103
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 65 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patients who have consented and recruited to the OptimiseII trial which includes
- •patients aged 65 years and over undergoing major elective surgery involving the gastrointestinal tract that is expected to take longer than 90 minutes.
排除标准
- •Inability or refusal to provide patient consent
- •clinician refusal (including intention to monitor cardiac output from the start of surgery regardless of study group allocation)
- •American Society of Anesthesiologists (ASA) score of I
- •patients expected to die within 30 days
- •acute myocardial ischaemia within 30 days prior to randomisation
- •acute pulmonary oedema within 30 days prior to randomisation
- •contra-indication to low-dose inotropic medication
- •pregnancy at time of enrolment
- •current participation in another clinical trial of a treatment with a similar biological mechanism or primary outcome measure
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