TCTR20230524003招募中4 期
Comparing effect of intravenous parecoxib for acute pain management before and after incision in total abdominal hysterectomy
Makarak Hospital0 个研究点目标入组 60 人开始时间: 2023年5月24日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 60
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. 18-65 years old
- •2. total abdominal hysterectomy operation, midline incision
- •3. no underlyling disease eg. myocardial infarction, congestive heart failure, GI bleeding, stroke
- •4. no drug allergy to parecoxib, NSAIDs, sulfonamides, aspirin and bupivacaine
- •5. serum creatinine < 1.5 mg/dL
- •6. no hepatic failure(Child-Pugh Class C)
排除标准
- •1. withdrawal from this study
- •2. operation under general anesthesia
研究者
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