首页> 美国卫生研究院文献>BMJ Open >Clinical efficacy and mechanistic evaluation of aflibercept for proliferative diabetic retinopathy (acronym CLARITY): a multicentre phase IIb randomised active-controlled clinical trial
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Clinical efficacy and mechanistic evaluation of aflibercept for proliferative diabetic retinopathy (acronym CLARITY): a multicentre phase IIb randomised active-controlled clinical trial

机译:阿柏西普治疗增生性糖尿病视网膜病变的临床疗效和机理评估(缩写CLARITY):一项多中心IIb期随机对照研究

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摘要

IntroductionProliferative diabetic retinopathy (PDR) is the main cause of severe visual loss in people with diabetes mellitus. The standard treatment for this condition is panretinal photocoagulation (PRP). This laser treatment is inherently destructive, with predictable adverse effects on visual function, and a safer alternative is required. Intravitreal injection of vascular endothelial growth factor (VEGF) inhibitors can induce short-term regression of retinal neovascularisation. The aim of this randomised controlled trial is to determine the efficacy, safety and cost-effectiveness of intravitreal aflibercept, an inhibitor of VEGF-A, VEGF-B and placental growth factor (PLGF), in PDR, and to investigate the impact on local oxygenation.
机译:简介糖尿病性视网膜增生症(PDR)是糖尿病患者严重视力丧失的主要原因。这种情况的标准治疗方法是全视网膜光凝(PRP)。这种激光治疗具有破坏性,对视觉功能具有可预见的不利影响,因此需要更安全的替代方法。玻璃体内注射血管内皮生长因子(VEGF)抑制剂可引起视网膜新生血管的短期消退。这项随机对照试验的目的是确定玻璃体腔注射阿柏西普(VEGF-A,VEGF-B和胎盘生长因子(PLGF)的抑制剂)在PDR中的疗效,安全性和成本效益,并研究其对局部用药的影响氧合。

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