ACTRN12609000966291已完成4 期
In patients with acute low back pain is time contingent paracetamol, or pro re nata (PRN) paracetamol, more effective than placebo in speeding recovery from a new episode of low back pain?
The George Institute for International Health0 个研究点目标入组 1,650 人开始时间: 2009年11月9日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1,650
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
- 16 Years 至 o limit（—）
- 性别
- All
入选标准
- •Primary complaint of pain in the area between the 12th rib and buttock crease, with/without leg pain;
- •New episode of low back pain, preceded by a period of at least one month without low back pain;
- •Pain of less than 6 weeks duration;
- •Low back pain severe enough to cause at least ‘moderate pain’ (as measured by an adaptation of item 7 of the Short Form-36).
排除标准
- •Known or suspected serious spinal pathology;
- •Currently taking recommended regular doses of paracetamol;
- •Currenlty taking recommended regular doses of another analgesic for a pre-existing condition;
- •Spinal surgery within the preceding 6 months;
- •Currently taking psychotropic medication and whose health condition is considered to prevent reliable recording of study information;
- •Serious co-morbidities preventing prescription of paracetamol;
- •Pregnancy or planning a pregnancy during the one-month treatment period.
研究者
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