ACTRN12609000555257已完成未知
A randomised controlled trial comparing pain scores for rectal Diclofenac with oral Diclofenac and oral or rectal Paracetamol in primiparous women after childbirth.
orthern Sydney & Central Coast Health, Human Research Ethics Committee0 个研究点目标入组 240 人开始时间: 2009年7月8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
- 240
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •Primiparous women who have a second-degree tear or greater or an episiotomy after a vaginal birth.
排除标准
- •Contraindications to non-steroidal anti-inflammatory medications
- •History of gastrointestinal ulcer or bleeding
- •Significant renal or liver impairment
- •Preeclampsia and essential hypertension.
- •Postpartum haemorrhage greater than 1000mL
- •Medical disorders associated with a disturbed coagulation profile, in particular immune thrombocytopenic purpura, disseminated intravascular coagulation
- •Women of non-English speaking background
- •Women taking anticoagulants, Lithium, Digoxin, Chloramphenicol or diuretics
研究者
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