TCTR20160109001招募中2 期
Efficacy of celecoxib for pain relief and antipyresis in pregnant women receiving misoprostol for termination of pregnancy
Songkhlanakarind hospital0 个研究点目标入组 64 人开始时间: 2016年1月9日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 64
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
- 0 N/A (No limit) 至 0 Years（—）
- 性别
- Female
入选标准
- •Women with intrauterine pregnancy requesting therapeutic abortion for any indications and Gestational age 14-24 weeks which is confirmed by USG
排除标准
- •- Allergy to NSAIDs/Sulfa
- •- Contraindicate for Celecoxib
- •- History of fever, PROM, vaginal bleeding, abdominal pain
- •- History of previous induced abortion by medication or devices
研究者
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