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Acupuncture for post anaesthetic recovery and postoperative pain: study protocol for a randomised controlled trial

机译:针刺麻醉后恢复和术后疼痛:一项随机对照试验的研究方案

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Background We report on the design and implementation of a study protocol entitled Acupuncture randomised trial for post anaesthetic recovery and postoperative pain - a pilot study (ACUARP) designed to investigate the effectiveness of acupuncture therapy performed in the perioperative period on post anaesthetic recovery and postoperative pain. Methods/Design The study is designed as a randomised controlled pilot trial with three arms and partial double blinding. We will compare (a) press needle acupuncture, (b) no treatment and (c) press plaster acupressure in a standardised anaesthetic setting. Seventy-five patients scheduled for laparoscopic surgery to the uterus or ovaries will be allocated randomly to one of the three trial arms. The total observation period will begin one day before surgery and end on the second postoperative day. Twelve press needles and press plasters are to be administered preoperatively at seven acupuncture points. The primary outcome measure will be time from extubation to ‘ready for discharge’ from the post anaesthesia care unit (in minutes). The ‘ready for discharge’ end point will be assessed using three different scores: the Aldrete score, the Post Anaesthetic Discharge Scoring System and an In-House score. Secondary outcome measures will comprise pre-, intra- and postoperative variables (which are anxiety, pain, nausea and vomiting, concomitant medication). Discussion The results of this study will provide information on whether acupuncture may improve patient post anaesthetic recovery. Comparing acupuncture with acupressure will provide insight into potential therapeutic differences between invasive and non-invasive acupuncture techniques. Trial registration NCT01816386 (First received: 28 October 2012)
机译:背景我们报道了一项关于麻醉后恢复和术后疼痛的针灸随机试验研究方案的设计和实施情况-一项旨在研究围手术期针灸治疗对麻醉后恢复和术后疼痛的有效性的中试研究(ACUARP) 。方法/设计本研究设计为三臂和部分双盲的随机对照试验。我们将比较(a)按针针灸,(b)未治疗和(c)按标准麻醉剂按石膏针压法。计划将75例接受腹腔镜子宫或卵巢手术的患者随机分配到三个试验组之一。整个观察期将在手术前一天开始,并在术后第二天结束。术前应在七个穴位注射十二个按针和按膏药。主要结果指标是从拔管到麻醉后护理部门“准备出院”的时间(以分钟为单位)。 “出院准备就绪”终点将使用三个不同的分数进行评估:Aldrete分数,麻醉后出院评分系统和室内分数。次要结局指标将包括术前,术中和术后变量(焦虑,疼痛,恶心和呕吐,伴随用药)。讨论这项研究的结果将提供有关针灸是否可以改善患者麻醉后恢复的信息。将针灸与针灸进行比较,将有助于洞悉有创和无创针灸技术之间的潜在治疗差异。试用注册号NCT01816386(首次收到:2012年10月28日)

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