TCTR20171115001已完成4 期
Analgesic Efficacy of Intravenous Nefopam after Spine Surgery: A Randomized, Double-Blind, Placebo-Controlled Trial
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 96
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 0 N/A (No limit)（—）
- 性别
- All
入选标准
- •1. Age ≥ 18 years
- •2. Scheduled for lumbosarcral spine surgery under general anesthesia
- •3. ASA physical status I - III
- •4. Operation time 4 - 6 hours
- •5. Not known allergy to morphine and nefopam
排除标准
- •1. Current nefopam use within 24 hours prior to study
- •2. Previous history of cardiovascular disease
- •3. Previous history of epilepsy
- •4. Previous history of liver disease
- •5. Previous history of chronic opioids therapy > 2 weeks
- •6. Previous history of chronic Monoamine oxidase inhibitors (MAOIs) therapy > 2 weeks
- •7. Unable to use patient controlled analgesia (PCA) device
- •8. Creatinine clearance < 30 mL/min (calculated by the Cockcroft-Gault equation)
研究者
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