TCTR20150320001已完成4 期
Effect of parecoxib intravenous administered compared with bupivacaine local infiltration in post surgical pain management following total abdominal hysterectomy
Department of Obstetrics and Gynecology, Faculty of Medicine Ramathibodi Hospital0 个研究点目标入组 42 人开始时间: 2015年3月20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
- 42
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 60 Years（—）
- 性别
- Female
入选标准
- •age 18-60 yr
- •undergoing total abdominal hysterrectomy
- •ASA status I-II
排除标准
- •BMI > 30 kg/m2
- •known case or suspected OSA
- •history of MI or CHF
- •history of GI bleeding
- •drug allergy to parecoxib, NSAIDs, bupivacaine
- •mental or physical inability to use PCA
- •serum creatinine > 1.5 mg/dL
- •severe liver disease ( Child-Pugh Class C)
研究者
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