跳至主要内容
临床试验/NCT01608113
NCT01608113Unknown不适用

Long-term Follow-up of Subfoveal Neovascular AMD

Medical University of Vienna1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2011年9月最近更新:
适应症

试验速览

阶段
不适用
入组人数
70
试验地点
1
主要终点
Long-term visual function performance

研究概览

简要总结

Treatment naive patients with subfoveal nAMD initially treated monthly with intravitreal anti-VEGF and subsequently PRN, will be included in this study. Patients will be investigated for the first 2 years monthly and subsequently according to disease activity but at least every two months. Patients will be examined with 4m BCVA ETDRS distance visual acuity, reading acuity measured by Radner-Reading-Charts, contrast sensitivity by Pelli-Robson score, microperimetry and HD-OCT.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • treatment naive subfoveal AMD, written informed consent, able to read

排除标准

  • choroidal neovascularisation due to other ocular diseases, mature cataract

结局指标

主要结局

Long-term visual function performance

时间窗: four years

次要结局

  • change of morphological alterations assessed by SD-OCT(four years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Christopher Kiss

Head of Vienna Study Center

Medical University of Vienna

研究点 (1)

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