TCTR20170809002已完成4 期
The efficacy of preemptive gabapentin for pain reduction after gynecologic surgery
none0 个研究点目标入组 36 人开始时间: 2017年8月9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
- 36
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 65 Years（—）
- 性别
- Female
入选标准
- •1)body mass index below or equal 35 kg/m2
- •3)American Society of Anesthesiologists physical status (ASA) classification class I-II
- •4)Appointment to explore laparotomy for gynecologic surgery include total abdominal hysterectomy(TAH) with or without oophorectomy, salpingectomy, omentectomy, or lymphadenectomy
- •5)General anesthesia
- •6)Understand and can use visual analogue scale (VAS)
- •7)Understand and can use patient controlled analgesia (PCA)
排除标准
- •1)Allery to gabapentin or opioid
- •2)underlying disease of epilepsy, psychiatric disease, or chronic pain
- •3)Use addictive substance or analgesic within 48 hours before surgery
- •4)Ovarian or fallopian tube cancer
- •5)Expect for long operation than 4 hours
研究者
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