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Statistical analysis plan for the Laser-1st versus Drops-1st for Glaucoma and Ocular Hypertension Trial (LiGHT): a multi-centre randomised controlled trial

机译:青光眼和高眼压试验(LaGHT)的Laser-1st与Drops-1st的统计分析计划:一项多中心随机对照试验

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Background The LiGHT trial (Laser-1st versus Drops-1st for Glaucoma and Ocular Hypertension Trial) is a multicentre randomised controlled trial of two treatment pathways for patients who are newly diagnosed with open-angle glaucoma (OAG) and ocular hypertension (OHT). The main hypothesis for the trial is that lowering intraocular pressure (IOP) with selective laser trabeculoplasty (SLT) as the primary treatment (‘Laser-1st’) leads to a better health-related quality of life than for those started on IOP-lowering drops as their primary treatment (‘Medicine-1st’) and that this is associated with reduced costs and improved tolerability of treatment. This paper describes the statistical analysis plan for the study. Methods/Design The LiGHT trial is an unmasked, multi-centre randomised controlled trial. A total of 718 patients (359 per arm) are being randomised to two groups: medicine-first or laser-first treatment. Outcomes are recorded at baseline and at 6-month intervals up to 36?months. The primary outcome measure is health-related quality of life (HRQL) at 36?months measured using the EQ-5D-5L. The main secondary outcome is the Glaucoma Utility Index. We plan to analyse the patient outcome data according to the group to which the patient was originally assigned. Methods of statistical analysis are described, including the handling of missing data, the covariates used in the adjusted analyses and the planned sensitivity analyses. Trial registration The trial was registered with the ISRCTN register on 23/07/2012, number ISRCTN32038223 .
机译:背景LiGHT试验(青光眼和高眼压试验的Laser-1st和Drops-1st)是一项多中心随机对照试验,针对新诊断为开角型青光眼(OAG)和高眼压(OHT)的患者采用两种治疗途径。该试验的主要假设是,以选择性激光小梁成形术(SLT)作为主要治疗方法(“ Laser-1st”)降低眼压(IOP)会导致与健康相关的生活质量优于降低IOP的患者作为主要治疗药物('Medicine-1st')下降,这与降低成本和提高治疗耐受性有关。本文介绍了这项研究的统计分析计划。方法/设计LiGHT试验是一项无掩盖的多中心随机对照试验。总共718名患者(每臂359名)被随机分为两组:药物优先或激光优先治疗。结果以基线记录,每6个月间隔一次,最长36个月。主要结局指标是使用EQ-5D-5L进行的36个月大的健康相关生活质量(HRQL)。主要的次要结果是青光眼效用指数。我们计划根据最初分配患者的组来分析患者结果数据。描述了统计分析的方法,包括缺失数据的处理,调整后的分析中使用的协变量以及计划的敏感性分析。试验注册该试验已于2012年7月23日在ISRCTN寄存器中注册,编号为ISRCTN32038223。

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