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临床试验/ISRCTN77853517
ISRCTN77853517已完成未知

Ocular discomfort following use of artificial tears in patients under treatment of intravitreal injections of anti-vascular endothelial growth factor agents

Oftalmología Vistahermosa S0 个研究点目标入组 34 人开始时间: 2021年2月17日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
34

研究概览

简要总结

2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36474999/ (added 08/12/2022)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Current inclusion criteria as of 06/04/2021:
  • 1. Patients with anti-vascular endothelial growth treatment with Lucentis 10mg/ml (ranibizumab, Novartis) for age-related macular degeneration
  • 2. Patients must have already received a minimum of three injections of this treatment
  • 3. Age between 51 and 90 years
  • Previous inclusion criteria:
  • 1. Patients with anti-vascular endothelial growth treatment with Lucentis 10mg/ml (ranibizumab, Novartis) for age-related macular degeneration
  • 2. Patients must have already received a minimum of three injections of this treatment
  • 3. Age between 50 and 90 years

排除标准

  • 1. Glaucoma
  • 2. Dry eye
  • 3. Previous refractive surgery or recent cataract surgery (less than 6 months)

研究者

发起方
Oftalmología Vistahermosa S

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