NCT00279487已完成不适用
Preanalgesic Effect of Gabapentin in Total Knee Repair
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 24
- 试验地点
- 1
研究概览
简要总结
The purpose of this study is to determine whether gabapentin, as a one time administration prior to a total knee replacement procedure, has opioid sparing effects and a reduction in pain scores.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients undergoing total knee replacement who received pain management by the following modality:
- •Intravenous patient-controlled analgesia (IV-PCA) opioid
- •Local femoral nerve block with 1.5% mepivacaine 20 ml and 0.5% ropivacaine 20 ml
排除标准
- •Age < 18 years old
研究组 & 干预措施
Arm 1
Active Comparator
Patients will receive 1200mg gabapentin 1-2 hours prior to surgery.
干预措施: Gabapentin (Drug)
Arm 2
Placebo Comparator
Patients will receive placebo 1-2 hours prior to surgery.
干预措施: Placebos (Drug)
研究者
研究点 (1)
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