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

被引:11
作者
Vickerstaff, Victoria [1 ,2 ]
Ambler, Gareth [3 ]
Bunce, Catey [4 ,5 ]
Xing, Wen [4 ,5 ]
Gazzard, Gus [4 ,5 ]
机构
[1] UCL, UCL Div Psychiat, Marie Curie Palliat Care Res Dept, London W1T 7NF, England
[2] UCL, Res Dept Primary Care & Populat Hlth, London NW3 2PF, England
[3] UCL, Dept Stat Sci, London WC1E 6BT, England
[4] Moorfields Eye Hosp, NIHR Biomed Res Ctr Ophthalmol, London, England
[5] UCL Inst Ophthalmol, London, England
关键词
Ophthalmology; open-angle glaucoma; ocular hypertension; randomised clinical trial; statistical analysis plan; QUALITY-OF-LIFE; OPEN-ANGLE GLAUCOMA; MEDICATION DELAYS; PREVENTS;
D O I
10.1186/s13063-015-1047-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
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页数:5
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