Newcastle Clinical Trials Unit, Newcastle University, Newcastle upon Tyne, NE2 4AE, UK.
Institute of Health and Society, Newcastle University, Newcastle upon Tyne, NE2 4AX, UK.
Trials. 2020 Feb 13;21(1):179. doi: 10.1186/s13063-020-4081-1.
Septoplasty (surgery to straighten a deviation in the nasal septum) is a frequently performed operation worldwide, with approximately 250,000 performed annually in the US and 22,000 in the UK. Most septoplasties aim to improve diurnal and nocturnal nasal obstruction. The evidence base for septoplasty clinical effectiveness is hitherto very limited.
To establish, and inform guidance for, the best management strategy for individuals with nasal obstruction associated with a deviated septum.
METHODS/DESIGN: A multicentre, mixed-methods, open label, randomised controlled trial of septoplasty versus medical management for adults with a deviated septum and a reduced nasal airway. Eligible patients will have septal deflection visible at nasendoscopy and a nasal symptom score ≥ 30 on the NOSE questionnaire. Surgical treatment comprises septoplasty with or without reduction of the inferior nasal turbinate on the anatomically wider side of the nose. Medical management comprises a nasal saline spray followed by a fluorinated steroid spray daily for six months. The recruitment target is 378 patients, recruited from up to 17 sites across Scotland, England and Wales. Randomisation will be on a 1:1 basis, stratified by gender and severity (NOSE score). Participants will be followed up for 12 months post randomisation. The primary outcome measure is the total SNOT-22 score at 6 months. Clinical and economic outcomes will be modelled against baseline severity (NOSE scale) to inform clinical decision-making. The study includes a recruitment enhancement process, and an economic evaluation.
The NAIROS trial will evaluate the clinical effectiveness and cost-effectiveness of septoplasty versus medical management for adults with a deviated septum and symptoms of nasal blockage. Identifying those individuals most likely to benefit from surgery should enable more efficient and effective clinical decision-making, and avoid unnecessary operations where there is low likelihood of patient benefit.
EudraCT: 2017-000893-12, ISRCTN: 16168569. Registered on 24 March 2017.
鼻中隔成形术(矫正鼻中隔偏曲的手术)是一项在全球范围内广泛开展的手术,美国每年约进行 25 万例,英国约进行 2.2 万例。大多数鼻中隔成形术旨在改善白天和夜间的鼻腔阻塞。迄今为止,鼻中隔成形术临床效果的证据基础非常有限。
确定并为鼻中隔偏曲相关鼻塞患者的最佳治疗策略提供依据。
方法/设计:一项多中心、混合方法、开放性标签、随机对照试验,比较鼻中隔成形术与药物治疗成人鼻中隔偏曲伴鼻腔气道狭窄。合格的患者将在鼻内镜下可见鼻中隔偏曲,NOSE 问卷的鼻腔症状评分≥30 分。手术治疗包括鼻中隔成形术,如有需要,还可在鼻腔较宽侧的下鼻甲进行鼻甲成形术。药物治疗包括鼻腔生理盐水喷雾,然后每天使用氟替卡松喷雾,持续 6 个月。招募目标是 378 名患者,来自苏格兰、英格兰和威尔士的 17 个地点。将按照 1:1 的比例,按性别和严重程度(NOSE 评分)分层进行随机分组。参与者将在随机分组后 12 个月进行随访。主要结局指标是 6 个月时的总 SNOT-22 评分。临床和经济结局将根据基线严重程度(NOSE 量表)进行建模,以指导临床决策。该研究包括一个增强招募的过程和一个经济评估。
NAIROS 试验将评估鼻中隔成形术与药物治疗成人鼻中隔偏曲伴鼻塞症状的临床效果和成本效果。确定最有可能从手术中获益的个体,应该能够实现更高效和有效的临床决策,并避免在患者获益可能性低的情况下进行不必要的手术。
EudraCT:2017-000893-12,ISRCTN:16168569。于 2017 年 3 月 24 日注册。