首页> 外文OA文献 >A multicentre phase III randomised controlled single-masked clinical trial evaluating the clinical efficacy and safety of light-masks at preventing dark-adaptation in the treatment of early diabetic macular oedema (CLEOPATRA):study protocol for a randomised controlled trial
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A multicentre phase III randomised controlled single-masked clinical trial evaluating the clinical efficacy and safety of light-masks at preventing dark-adaptation in the treatment of early diabetic macular oedema (CLEOPATRA):study protocol for a randomised controlled trial

机译:一项多中心III期随机对照单掩盖临床试验,评估遮光膜在预防早期糖尿病性黄斑水肿(CLEOPATRA)中的适应性和预防黑暗适应性的临床疗效和安全性:一项随机对照试验的研究方案

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摘要

BACKGROUND: This study will evaluate hypoxia, as a novel concept in the pathogenesis of diabetic macular oedema (DMO). As the oxygen demand of the eye is maximum during dark-adaptation, we hypothesize that wearing light-masks during sleep will cause regression and prevent the development and progression of DMO. The study protocol comprises both an efficacy and mechanistic evaluation to test this hypothesis.METHOD/DESIGN: This is a phase III randomised controlled single-masked multicentre clinical trial to test the clinical efficacy of light-masks at preventing dark-adaptation in the treatment of non-central DMO. Three hundred patients with non-centre-involving DMO in at least one eye will be randomised 1:1 to light-masks and control masks (with no light) to be used during sleep at night for a period of 24 months. The primary outcome is regression of non-central oedema by assessing change in the zone of maximal retinal thickness at baseline on optical coherence tomography (SD-OCT). Secondary outcomes will evaluate the prevention of development and progression of DMO by assessing changes in retinal thickness in different regions of the macula, macular volume, refracted visual acuity and level of retinopathy. Safety parameters will include sleep disturbance. Adverse events and measures of compliance will be assessed over 24 months. Participants recruited to the mechanistic sub-study will have additional retinal oximetry, multifocal electroretinography (ERG) and microperimetry to evaluate the role of hypoxia by assessing and comparing changes induced by supplemental oxygen and the light-masks at 12 months.DISCUSSION: The outcomes of this study will provide insight into the pathogenesis of DMO and provide evidence on whether a simple, non-invasive device in the form of a light-mask can help prevent the progression to centre-involving DMO and visual impairment in people with diabetes.
机译:背景:本研究将评估缺氧,将其作为糖尿病性黄斑水肿(DMO)发病机理的新概念。由于在黑暗适应过程中眼睛的氧气需求量最大,因此我们假设在睡眠过程中戴口罩会导致退化,并阻止DMO的发生和发展。研究方案包括功效和机制评估,以检验该假设。方法/设计:这是一项III期随机对照单掩蔽多中心临床试验,旨在检验光罩在预防暗适应治疗中的临床功效。非中央DMO。 300例至少有一只眼睛不涉及中心的DMO患者将按照1:1的比例随机分配到光罩和对照罩(不带灯),以便在夜间睡眠期间使用,持续24个月。主要结果是通过在光学相干断层扫描(SD-OCT)上评估基线时最大视网膜厚度区域的变化来消退非中心性水肿。次要结果将通过评估黄斑不同区域的视网膜厚度,黄斑体积,屈光视力和视网膜病变水平来评估DMO的发生和发展的预防。安全参数将包括睡眠障碍。不良事件和遵守措施将在24个月内进行评估。招募至该机制子研究的参与者将进行额外的视网膜血氧饱和度测定,多焦点视网膜电图(ERG)和显微视野测定,以通过评估和比较补充氧和光罩在12个月时引起的变化来评估缺氧的作用。这项研究将提供有关DMO发病机理的见解,并提供证据证明简单,无创的光罩形式的设备是否可以帮助预防糖尿病患者发展为涉及中心的DMO和视力障碍。

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