ACTRN12611000345987已完成4 期
Early postoperative analgesia from parecoxib, paracetamol or both among patients having minor gynaecological sugery
Women's and Newborn Health Service0 个研究点目标入组 240 人开始时间: 2011年4月1日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 70 Years（—）
- 性别
- Female
入选标准
- •Dilatation and curettage
- •American Society of Anesthesiologists physical status 1 or 2
排除标准
- •Renal dysfunction
- •Hypertension
- •Ischaemic heart disease
- •Cerebrovascular disease
- •Peptic ulcer or gastro-intestinal reflux disease
- •Aspirin or nonsteroidal anti-inflammatory drug induced asthma
- •Allergy to paracetamol, parecoxib or sulphonamides
- •Hepatic dysfunction
- •Taking analgesic drugs within 24 hours of surgery
- •Unsuitable for anaesthesia with volatile anaesthetics or requiring intubation
- •Prophylactic antiemetic therapy indicated
研究者
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