首页> 美国卫生研究院文献>BMC Ophthalmology >Efficacy of a fixed combination of 0.09  xanthan gum/0.1  chondroitin sulfate preservative free vs polyethylene glycol/propylene glycol in subjects with dry eye disease: a multicenter randomized controlled trial
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Efficacy of a fixed combination of 0.09  xanthan gum/0.1  chondroitin sulfate preservative free vs polyethylene glycol/propylene glycol in subjects with dry eye disease: a multicenter randomized controlled trial

机译:固定组合0.09%黄原胶/0.1硫酸软骨素防腐剂对聚乙二醇/丙二醇的治疗对干眼症的疗效:一项多中心随机对照试验

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摘要

BackgroundDry eye disease (DED) is multifactorial, affecting 5–34 % of the global adult population and reducing quality of life. The artificial tears or lubricants are the therapy most used for the treatment of DED, due to their low side effect profile, which attempt to modify the properties of the tear film. The aim of the present study was to evaluate the clinical efficacy of a fixed combination of xanthan gum and chondroitin sulfate preservative free on the ocular surface of patients with dry eye disease during 60 days of intervention.
机译:背景干眼病(DED)是多因素的,影响了全球成年人口的5–34%,并降低了生活质量。人造眼泪或润滑剂由于其副作用低,是最常用于治疗DED的疗法,其试图改变泪膜的性能。本研究的目的是评估干预期60天黄原胶和硫酸软骨素防腐剂固定组合在干眼病患者眼表上的临床疗效。

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