TCTR20190109003尚未招募3 期
Prosperity of celecoxib for pain relief after elective cesarean section delivery, a double-blind randomized controlled trial
/A0 个研究点目标入组 100 人开始时间: 2019年1月9日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
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 40 Years（—）
- 性别
- Female
入选标准
- •-term prgnancy
- •-singleton
- •-age 20 †40 year-old
- •-elective cesarean section or cesarean section with tubal sterilization
- •-Pfannenstiel incision
- •-spinal block
- •-BMI < 35 kg/mm2
排除标准
- •No history of NSAIDs,sulfa group and opioid groug allery
- •No liver,hematology,renal and heart disease
- •No currently warfarin tak
- •Opertive time <= 2 hours
- •Blood loss<= 1000 ml
研究者
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