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Efficacy of acetaminophen with and without oxycodone for analgesia in non-operative treatment of extremity fractures in adults: protocol for a double-blind randomized clinical trial

机译:对乙酰氨基酚联合或不联合羟考酮对成人肢端骨折非手术治疗的镇痛效果:一项双盲随机临床试验的方案

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Opioids and acetaminophen are both widely used to relieve pain after non-operative treatment of limb fractures, but evidence for the superiority of opioids versus acetaminophen is lacking. In this study, we aim to determine whether acetaminophen is non-inferior to the acetaminophen/oxycodone combination for pain relief after non-operative fixation of an extremity limb fracture. We hypothesize that acetaminophen is non-inferior to the acetaminophen/oxycodone combination. A double-blind randomized controlled trial will be conducted. Power analysis determined that 1226 participants will be needed (P?0.05, power 90%). Patients with acute limb fracture who receive non-operative treatment will be recruited and randomly allocated into two groups: the intervention group will receive oral oxycodone (10?mg) and acetaminophen (650?mg), and the control group will receive acetaminophen (650?mg) only. All participants will be instructed to take one pill of study medication on an as-needed basis and no more frequently than once every 8?h. The primary outcome measure will be scores on the 11-point Numeric Rating Scale (NRS-11) over 14?days. Secondary outcome measures are scores on the Self-Rating Anxiety Scale (SAS), Self-Rating Depression Scale (SDS), EuroQol five-dimension questionnaire (EQ-5D), self-rated satisfaction with the analgesia produced, self-reported nighttime sleep duration, number of intervention or control pills used, and total duration for taking intervention or control medication. Change of pain scores and the number of times that analgesic drugs were taken in the two groups will be statistically evaluated with Student t tests according to their fracture site. This study will be a randomized controlled trial that is adequately powered to test the hypothesis that acetaminophen is non-inferior to the combination of acetaminophen and oxycodone in relieving objectively measured pain after non-operative treatment of limb fractures in adults. It will hopefully provide a safe and effective analgesic plan for such patients. ChiCTR registry: ChiCTR1800017015 . Registered on July 8, 2018.
机译:非手术治疗肢体骨折后,阿片类药物和对乙酰氨基酚均被广泛用于缓解疼痛,但缺乏阿片类药物比对乙酰氨基酚优越的证据。在这项研究中,我们旨在确定对乙酰氨基酚是否不劣于对乙酰氨基酚/羟考酮组合以减轻非手术性固定肢体四肢骨折后的疼痛。我们假设对乙酰氨基酚不逊于对乙酰氨基酚/羟考酮组合。将进行双盲随机对照试验。功效分析确定需要1226名参与者(P <0.05,功效90%)。将招募接受非手术治疗的急性肢体骨折患者,并随机分为两组:干预组将接受口服羟考酮(10?mg)和对乙酰氨基酚(650?mg),对照组将对乙酰氨基酚(650) ?mg)。将指导所有参与者在需要时服用一粒研究药物,且每8?h不超过一次。主要结局指标为14天以11点数字评分量表(NRS-11)评分。次要结局指标包括:自评焦虑量表(SAS),自评抑郁量表(SDS),EuroQol五维问卷(EQ-5D),对镇痛产生的自我评价满意度,自我报告的夜间睡眠持续时间,使用的干预或对照药的数量以及服用干预或对照药物的总时间。两组疼痛评分的变化和止痛药的服用次数将根据其骨折部位进行Student t检验进行统计学评估。这项研究将是一项随机对照试验,该试验有足够的能力验证以下假设:对乙酰氨基酚不逊于对乙酰氨基酚和羟考酮的组合,可以缓解成人肢体骨折的非手术治疗后客观测量出的疼痛。希望它将为此类患者提供安全有效的镇痛方案。 ChiCTR注册表:ChiCTR1800017015。 2018年7月8日注册。

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