ISRCTN15165914已完成未知
A Feasibility Randomised Controlled Trial to compare REgional versus General Anaesthesia in Reducing Delirium in patients with Hip Fractures
niversity of Warwick0 个研究点目标入组 100 人开始时间: 2017年10月12日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Clinically or radiographically diagnosed intracapsular or extracapsular hip fracture
- •2. Planned surgical treatment via hemiarthroplasty, total hip arthroplasty or appropriate fixation procedure
- •3. Aged 65 years and over
排除标准
- •1. Multiple trauma or planned concurrent surgery not amenable to spinal anaesthesia
- •2. Absolute contraindication to regional anaesthesia:
- •2.1. Known or suspected congenital or acquired coagulopathy
- •2.2. Active use of pharmacological anticoagulants within a timeframe defined to contraindicate neuraxial block placement
- •2.3. Known or suspected unrepaired critical or severe aortic stenosis
- •2.4. Known or suspected active skin infection at the planned needle insertion site
- •2.5. Known or suspected elevated intracranial pressure contraindicating dural puncture; previous spinal surgery precluding RA, localised sepsis in lumbar spine, documented allergies to local anaesthetic
- •3. Known or suspected to be at elevated risk for malignant hyperthermia
- •4. Previous participation in the REGARD trial
- •5. Determination by the surgeon or the anaesthetist that the patient would not be suitable for randomisation
- •6. Patient not expected to survive beyond 48 hours
研究者
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