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临床试验/NCT06416241
NCT06416241已完成4 期

Intravitreal Aflibercept for Macular Edema Due to Central Retinal Vein Occlusion

University of Athens0 个研究点目标入组 51 人开始时间: 2017年1月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
51
主要终点
Change in retinal thickness as measured in μm using spectral domain optical coherence tomography

研究概览

简要总结

Central retinal vein occlusion (CRVO) is a common retinal vascular disorder, occurring when there is a blockage to the main blood vessel that transports blood away from the retina. CRVO may cause visual impairment, especially due to macular edema (swelling of the macula due to fluid accumulation) and macular non-perfusion.

Aflibercept has been found to improve visual acuity and reduce macular thickness in pivotal trials.

The purpose of this study was to evaluate the efficacy and safety of intravitreal aflibercept in real-world, using a patient-fitted treatment regimen. Additionally, imaging parameters have been assessed before and after treatment with intravitreal aflibercept.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Treatment naive center-involved macular edema secondary to CRVO for no longer than 3 months.
  • Patients >18 years of age, who are diagnosed with macular edema secondary to CRVO who are scheduled to be treated with intravitreal aflibercept in real-life conditions
  • BCVA of Snellen of 20/40 to 20/200 in the study eye

排除标准

  • Previous PRP or macular laser photocoagulation in the study eye.
  • Any prior ocular treatment in the study eye for macular edema secondary to CRVO.
  • Prior systemic anti-VEGF or corticosteroid therapy, within the last 3 months before enrollment to the study.
  • Any active or previous inflammation, ocular trauma
  • Uncontrolled glaucoma (IOP>30 mmHg)

研究组 & 干预措施

Eylea 2.0mg/0.05ml

Other

干预措施: EYLEA 2 MG in 0.05 ML Injection (Drug)

结局指标

主要结局

Change in retinal thickness as measured in μm using spectral domain optical coherence tomography

时间窗: 5 years

Change in visual acuity as measured using ETDRS charts

时间窗: 5 years

次要结局

  • Change in microvascular parameters in OCT angiography (vessel density, FAZ area)(2 years)
  • Complications(5 years)
  • Change in endothelial dysfunctionafter aflibercept treatment, as measured by the perfused boundary region sublingual 5-25 μm(6 months)

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

Associate Professor in Ophthalmology

National and Kapodistrian University of Athens

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