PACTR202201655513401尚未招募未知
Efficacy and safety of four-weeks versus twelve-weeks loading doses spacing of intravitreal Aflibercept for treatment of macular edema associated with Central Retinal Vein Occlusion
Egypt health insurance0 个研究点目标入组 60 人开始时间: 2022年1月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- All
入选标准
- •Any participant to be included in the study should have:
- •normal or controlled blood pressure.
- •normal Hba1c or controlled (maximum 6.5%).
- •normal or controlled lipogram.
- •Patients aged =18 years with center-involved macular edema due to CRVO (CMT =250 µm on OCT).
- •Best corrected visual acuity (BCVA) of 20/40 to 20/320 (73 to 24 letters)
排除标准
- •Exclusion criteria comprised the following:
- •pregnancy or lactation.
- •previous vitreoretinal or filtration surgery.
- •iris neovascularization.
- •any systemic or ocular disorder in the study eye that may confound the interpretation of the study results.
- •previous treatment with any anti-VEGF agents.
- •systemic anti-angiogenic medications.
- •intraocular corticosteroids
研究者
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