TCTR20170807002已完成4 期
Effectiveness of Perioperative Dexamethasone and Bupivacaine for Reducing Postoperative Pain in Posterior Lumbosacral Spine Surgery: A preliminary randomized double blind placebo-controlled trial
Department of Orthopaedics Faculty of Medicine Chiang Mai University0 个研究点目标入组 32 人开始时间: 2017年8月7日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 32
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
- 年龄范围
- 18 Years 至 70 Years（—）
- 性别
- All
入选标准
- •1.) Age ≥ 18
- •2.) ASA physical status I or II
- •3.) Can operate patient-controlled analgesia (PCA) device
- •4.) Degenerative condition of spinal disease
- •5.) No previous spinal surgery
排除标准
- •1.) Allergy to steroid or bupivacaine or morphine
- •2.) Prohibit to substance made from pig e.g. Muslim
- •3.) Pregnancy or lactating
- •4.) Infection, trauma or tumor spinal condition
- •5.) History previous spinal surgery
- •6.) Smoking
研究者
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