TCTR20140909001尚未招募未知
The study aims to investigate the effectiveness of parecoxib 40 mg in controlling pain after elective cesarean delivery. The subjects were divided into 2 groups: intervention and control group. The intervention includes pregnant women who age over 20
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 82
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
- 20 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •Pregnant women age over 20 years old
- •Admission of elective cesarean delivery
- •Anesthetic method is spinal anesthesia
排除标准
- •Contraindication to NSAIDs
- •Allergy to NSAIDs
- •Current medication is warfarin and antifungal drugs
研究者
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