ACTRN12608000088347尚未招募3 期
Can Pregabalin prevent persistent post amputation pain?
John Hunter Hospital-Hunter Integrated Pain Service0 个研究点目标入组 120 人开始时间: 2008年2月15日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 120
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 /A（—）
- 性别
- All
入选标准
- •Patient able to provide own informed consent.
- •there is sufficient ime before proposed surgery to allow absorption of loading dose of pregabalin, minimum 2hrs
- •Patient is suitable for standard general anaesthetic (GA) regimen and able to use patient controlled analgesia (PCA) for postop analgesia
排除标准
- •Current use of gabapentin
- •Unable to give consent
- •significant renal impairment
- •galactos metabolic disorders
研究者
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