IRCT201106136790N1已完成3 期
Comparing the efficacy of Ibuprofen and Celecoxib on the intensity of perineal pain following episiotomy: a single blind, randomized clinical trial
Ilam University of Medical Sciences0 个研究点目标入组 170 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 170
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 35 years（—）
- 性别
- Female
入选标准
- •1-18-35 y/o; 2-mediolateral episiotomy; 3-singleton; 4- alive fetus. Exclusion criteria: 1-sensitivity to NSAIDs; 2-history of digestive system disorders; 3-presence of chronic illness; 4-rupture of cervix; 5-post partum hemorrhage; 6-pre eclampcia and eclampcia; 7-PROM.
排除标准
- 未提供
研究者
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