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The effects of ventilation tubes versus no ventilation tubes for recurrent acute otitis media or chronic otitis media with effusion in 9 to 36?month old Greenlandic children, the SIUTIT trial: study protocol for a randomized controlled trial

机译:SIUTIT试验:对于9到36个月大的格陵兰儿童,复发性急性中耳炎或慢性中耳炎伴有积液的通气管与无通气管的影响,SIUTIT试验:一项随机对照试验的研究方案

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Background The prevalence of otitis media in Greenlandic children is one of the highest in the world. International studies have shown that otitis-prone children may benefit from tubulation of the tympanic membrane. However, it is unknown whether these results can be applied to Greenlandic children and trials on the effects of ventilation tubes in high-risk populations have, to our knowledge, never been conducted. Methods The trial is an investigator-initiated, multicentre, randomized, blinded superiority trial of bilateral ventilation tube insertion versus treatment as usual (no tube) in Greenlandic children aged 9–36 months with chronic otitis media with effusion or recurrent acute otitis media. With randomization stratified by otitis media subtype and trial site, a type 1 error of 5% and a power of 80%, a total of 230 participants are needed to detect a decrease of two visits to a health clinic during 2?years, which is considered the minimal clinical relevant difference. The primary outcome measure will be assessed blindly by investigating medical records. Secondary outcome measures are number of episodes of acute otitis media, quality of life, number of episodes of antibiotics administration and proportion of children with tympanic membrane perforations. Discussion This trial will provide evidence-based knowledge of the effects of ventilation tubes in children with middle ear infections from the high-risk Greenlandic population. Furthermore, this trial will improve the understanding of conducting randomized clinical trials in remote areas, where management of logistical aspects is particularly challenging. Trial registration ClinicalTrials.gov, NCT02490332 . Registered on 14 February 2016.
机译:背景格陵兰儿童中耳炎的患病率是世界上最高的疾病之一。国际研究表明,易患中耳炎的儿童可能会从鼓膜的输卵管中受益。然而,尚不清楚这些结果是否可用于格陵兰儿童,据我们所知,从未进行过有关高危人群通气管作用的试验。方法该试验是由研究者发起的一项多中心,随机,双盲优势试验,针对年龄在9–36个月的慢性中耳炎伴有积液或复发性急性中耳炎的格陵兰儿童进行双侧通气管插入与常规治疗(无管)比较。按中耳炎亚型和试验部位进行分层,类型1错误为5%,功效为80%,则总共需要230名参与者才能检测到2年内两次就诊诊所的减少。考虑了最小的临床相关差异。将通过调查病历来盲目评估主要结局指标。次要结局指标是急性中耳炎发作次数,生活质量,服用抗生素的发作次数以及鼓膜穿孔患儿的比例。讨论该试验将为高风险的格陵兰人人群的中耳感染儿童提供通气管效果的循证知识。此外,该试验将提高对在偏远地区进行后勤管理特别具有挑战性的偏远地区进行随机临床试验的理解。试用注册ClinicalTrials.gov,NCT02490332。 2016年2月14日注册。

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