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临床试验/ISRCTN28276860
ISRCTN28276860已完成未知

Can deep phenotyping using retinal images predict response to intravitreal aflibercept therapy in patients with neovascular age-related macular degeneration?

Moorfields Eye Hospital0 个研究点目标入组 3,000 人开始时间: 2019年8月27日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
3,000

研究概览

简要总结

2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37109349/ (added 17/07/2023)

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Inclusion criteria for both retrospective and prospective parts:
  • 1. Adults who are = 50 years and = 100 years
  • 2. Treatment naïve neovascular AMD at baseline
  • 3. Media clarity, pupillary dilation and patient cooperation for adequate imaging
  • 4. Ability to give informed consent
  • Inclusion criteria for retrospective part only in addition to the above:
  • 1. Have received 3 loading injections of intravitreal aflibercept therapy at monthly intervals as per standard care
  • 2. Review up to 10 weeks after the 3rd loading dose with or without injection at this visit
  • 3. Had Heidelberg OCT at least at baseline and after the loading phase but ideally 4 Heidelberg OCTs for the 4 visits
  • 4. Heidelberg OCTA images if available for baseline and any visit thereafter (2nd, 3rd or 4th visit) provided there is a baseline OCTA (optional criteria)

排除标准

  • 1. Co-existent ocular disease: any other ocular condition that, in the opinion of the investigator, might affect or alter visual acuity during the course of the study
  • 2. Any patient who has opted out of their information being used for research nationally or locally at any site

研究者

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