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临床试验/NCT05683912
NCT05683912已完成不适用

Aflibercept for Diabetic Macular Edema In Real-life Practice in GREece: The ADMIRE Study

University of Athens1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年9月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
Change in best-corrected visual acuity

研究概览

简要总结

ADMIRE was a prospective, observational cohort study of patients with diabetic macular edema (DME). Efficacy was assessed by change in best-corrected visual acuity (BCVA) and central retinal thickness (CRT) from baseline to months 12, 24 and 36 after treatment with intravitreal aflibercept in treatment-naïve patients and previously treated patients. Safety was evaluated by recording any patients-reported events.

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
45 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with DM, able to give written informed consent Patients with DME>320 μm, who need treatment

排除标准

  • Patients with other retinal diseases than DME Intraocular surgery within the last 6 months

结局指标

主要结局

Change in best-corrected visual acuity

时间窗: 12 months

次要结局

未报告次要终点

研究者

发起方
University of Athens
申办方类型
Other
责任方
Principal Investigator
主要研究者

Irini Chatziralli

Assistant Professor in Ophthalmology

University of Athens

研究点 (1)

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