TCTR20140618001已完成未知
Efficacy of a single intravenous venous dose of Parecoxib 40 mg for post-operative pain control after elective cesarean delivery: a double blind randomized controlled trial
Siriraj Routine to Research Unit0 个研究点目标入组 82 人开始时间: 2014年6月18日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 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
- •1 Term pregnancy aged over 20 years old
- •2 Previous cesarean delivery
- •3 Elective cesarean delivery
- •4 Analgesia planning is spinal block
- •5 Able to read and write Thai language
排除标准
- •1. Allergy to NSAIDs
- •2. Contraindication to NSAIDs use
- •3. Warfarin or azole drugs use
研究者
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