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临床试验/ACTRN12613001243707
ACTRN12613001243707已完成未知

A comparison of intravenous ibuprofen 800mg, parecoxib 40mg, parecoxib 80mg and placebo in female patients undergoing hysteroscopy +/- dilatation and curettage +/- mirena insertion as day case surgery - a comparison of analgesic efficacy, quality of recovery and incidence of opioid related side effects

Department of Anaesthesia and Pain Medicine, King Edward Memorial Hospital0 个研究点目标入组 280 人开始时间: 2013年11月13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
280

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 o limit(—)
性别
Female

入选标准

  • Undergoing hysteroscopy +/- dilatation and curettage +/- mirena insertion

排除标准

  • Renal dysfunction
  • Hypertension
  • Ischaemic heart disease
  • Cerebrovascular disease
  • Past or current peptic ulcer disease
  • Allergy to non-steroidal anti-inflammatory drugs
  • Aspirin or NSAID induced asthma
  • Hepatocellular insufficiency
  • Unsuitable for general anaesthesia with maintenance with inhalational agent

研究者

发起方
Department of Anaesthesia and Pain Medicine, King Edward Memorial Hospital

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