首页> 外文期刊>Trials >A multi-centre open-label randomised non-inferiority trial comparing watchful waiting to antibiotic treatment for acute otitis media without perforation in low-risk urban Aboriginal and Torres Strait Islander children (the WATCH trial): study protocol for a randomised controlled trial
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A multi-centre open-label randomised non-inferiority trial comparing watchful waiting to antibiotic treatment for acute otitis media without perforation in low-risk urban Aboriginal and Torres Strait Islander children (the WATCH trial): study protocol for a randomised controlled trial

机译:一项多中心开放标签的非劣效性非劣效性试验,比较了低危城市原住民和托雷斯海峡岛民儿童中不穿孔的急性中耳炎的观察等待与抗生素治疗的比较(WATCH试验):一项随机对照试验的研究方案

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Background Treatment guidelines recommend watchful waiting for children older than 2?years with acute otitis media (AOM) without perforation, unless they are at high risk of complications. The high prevalence of chronic suppurative otitis media (CSOM) in remote Aboriginal and Torres Strait Islander communities leads these children to be classified as high risk. Urban Aboriginal and Torres Strait Islander children are at lower risk of complications, but evidence to support the subsequent recommendation for watchful waiting in this population is lacking. Methods/Design This non-inferiority multi-centre randomised controlled trial will determine whether watchful waiting is non-inferior to immediate antibiotics for urban Aboriginal and Torres Strait Islander children with AOM without perforation. Children aged 2???16?years with AOM who are considered at low risk for complications will be recruited from six participating urban primary health care services across Australia. We will obtain informed consent from each participant or their guardian. The primary outcome is clinical resolution on day 7 (no pain, no fever of at least 38?°C, no bulging eardrum and no complications of AOM such as perforation or mastoiditis) as assessed by general practitioners or nurse practitioners. Participants and outcome assessors will not be blinded to treatment. With a sample size of 198 children in each arm, we have 80?% power to detect a non-inferiority margin of up to 10?% at a significance level of 5?%, assuming clinical improvement of at least 80?% in both groups. Allowing for a 20?% dropout rate, we aim to recruit 495 children. We will analyse both by intention-to-treat and per protocol. We will assess the cost- effectiveness of watchful waiting compared to immediate antibiotic prescription. We will also report on the implementation of the trial from the perspectives of parents/carers, health professionals and researchers. Discussion The trial will provide evidence for the safety and effectiveness of watchful waiting for the management of AOM in Aboriginal and Torres Strait Islander children living in urban settings who are considered to be at low risk of complications. Trial registration The trial is registered with Australia New Zealand Clinical Trials Registry ( ACTRN12613001068?752 ). Date of registration: 24 September 2013.
机译:背景治疗指南建议注意等待2岁以上的急性中耳炎(AOM)儿童而无穿孔,除非他们有很高的并发症风险。在偏远的原住民和托雷斯海峡岛民社区中,慢性化脓性中耳炎(CSOM)患病率很高,导致这些儿童被列为高危儿童。城市原住民和托雷斯海峡岛民儿童患并发症的风险较低,但缺乏支持随后建议在该人群中进行观察等待的证据。方法/设计该非劣效性多中心随机对照试验将确定对于没有穿孔的AOM都市原住民和托雷斯海峡岛民儿童,观察性等待是否不劣于即刻抗生素。将从澳大利亚的六家参与城市初级卫生保健服务中招募被认为患并发症风险低的2 ??? 16岁AOM儿童。我们将获得每个参与者或其监护人的知情同意。主要结果是由全科医生或护士从第7天起临床解决(无疼痛,无38°C以上的发热,鼓膜鼓鼓和AOM并发症,例如穿孔或乳突炎)。参与者和结果评估者不会盲目接受治疗。每个手臂样本量为198名儿童,我们有80%的能力可以检测到5%的显着性水平下的10 %%的非自卑性,假设两者的临床改善均至少达到80%组。考虑到20%的辍学率,我们的目标是招募495名儿童。我们将通过意向性治疗和每个方案进行分析。与即时抗生素处方相比,我们将评估观察等待的成本效益。我们还将从父母/护理人员,卫生专业人员和研究人员的角度报告试验的实施情况。讨论该试验将提供证据,证明居住在城市地区的原住民和托雷斯海峡岛民儿童中观察到的等待AOM管理的安全性和有效性,这些儿童被认为并发症的风险较低。试验注册该试验已在澳大利亚新西兰临床试验注册中心(ACTRN12613001068?752)注册。注册日期:2013年9月24日。

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