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临床试验/NCT03513172
NCT03513172已完成不适用

Hypotensive Efficacy of Topical Prophylaxis for Intraocular Pressure Spikes Following Intravitreal Injections of Anti-vascular Endothelial Growth Factor Agents

University of Toronto0 个研究点目标入组 55 人开始时间: 2016年12月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
55
主要终点
Change in Post-Injection Intraocular Pressure Spike

研究概览

简要总结

In this study, investigators will be examining the intraocular pressure lowering effect of brimonidine 0.15% when administered 20min prior to intravitreal anti-VEGF injection.

详细描述

A total of 55 consecutive patients undergoing anti-VEGF intravitreal injections (received ≥1 treatments) for age-related macular degeneration (AMD), diabetic macular edema (DME) or macula edema secondary to branch retinal vein occlusion (BRVO) will be prospectively recruited between December 2016 and July 2017. Patients will be randomly assigned based on a pre-determined allocation sequence to receive topical brimonidine tartrate 0.15% (Alphagan® P; Allergan, Inc) during either the first or second of two consecutive visits. A standard protocol for sterile preparation with topical 5% povidone-iodine solution will be followed. Pre-injection IOP measurements will be recorded prior to the instillation of dilating agents and brimonidine tartrate. A total of three IOP measurements will be taken by certified ophthalmic technicians at immediately after the injection (T0), 10 minutes after (T10) and 20 minutes after (T20) injection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Prevention
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • received ≥1 treatments for age-related macular degeneration (AMD), diabetic macular edema (DME) or macula edema secondary to branch retinal vein occlusion (BRVO)

排除标准

  • baseline diagnosis of glaucoma
  • baseline IOP during last visit of greater than 21 mmHg
  • ongoing use of topical medications (eg. corticosteroids)
  • pseudophakic with an anterior chamber intraocular lens
  • history of ocular conditions that may impact IOP (eg. pseudoexfoliation)
  • previous in-office (eg. laser peripheral iridotomy) and vitreoretinal surgical procedures (eg. pars plana vitrectomy).

研究组 & 干预措施

Brimonidine Pre-Administration During First Visit

Active Comparator

干预措施: topical brimonidine tartrate 0.15% (Alphagan® P; Allergan, Inc) (Drug)

Brimonidine Pre-Administration During Second Visit

Active Comparator

干预措施: topical brimonidine tartrate 0.15% (Alphagan® P; Allergan, Inc) (Drug)

结局指标

主要结局

Change in Post-Injection Intraocular Pressure Spike

时间窗: Change from immediately, 10 minutes and 20 minutes after injection

the intraocular pressure lowering effect of brimonidine 0.15% ophthalmic eye drop when administered 20 minutes prior to intravitreal anti-VEGF injection

次要结局

未报告次要终点

研究者

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

Tina Felfeli

Medical Student

University of Toronto

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