The Impact of Genetic Polymorphisms on Ranibizumab Treatment Outcomes in Wet Age-Related Macular Degeneration (AMD)
试验速览
- 阶段
- 不适用
- 入组人数
- 300
- 试验地点
- 2
- 主要终点
- Visual acuity
研究概览
简要总结
Genetic factors of an individual patient may have an impact on Ranibizumab (Lucentis) treatment outcome in patients with Wet Age-Related Macular Degeneration (AMD).
详细描述
Age-Related Macular Degeneration (AMD) is a disease that affects central part of the retina, called macula, and is associated with progressive central vision loss. Moreover, AMD is known to be a leading cause of blindness in developed countries. In wet form of AMD, new abnormal blood vessels start to grow from the choroid towards the retina that leads to leakage from these vessels and, in turn, to impaired retinal structure and rapid vision loss.
Genetic factors were found to be important in development of wet AMD. Our previous research showed the association between some genetic polymorphisms and the risk of wet AMD as well as with specific clinical features of the disease. At present, anti-vascular endothelial growth factor (anti-VEGF) therapy with intravitreous ranibizumab (Lucentis) is considered to be the most effective treatment for wet AMD. However, treatment outcomes may vary significantly from improved vision to no effect. The aim of this research is to study how ranibizumab treatment outcomes depend on genetic factors.
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
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must be at least 50 years old
- •Neovascular age-related macular degeneration
- •CNV in the central part of the retina (macular is involved)
- •Active CNM (seen on fundus fluorescein angiography)
- •CNV activity is on one of the following: sub-retinal hemorrhage, sub-retinal lipid, documented loss of 3 lines of vision during last 3 months
- •Visual acuity of between 20/40 and 20/300 (ETDRS)
排除标准
- •Patients under 50 years old
- •Patients with CNM not caused by AMD
- •Patients physically unable to tolerate intravenous fluorescein angiography
- •Patients with medically uncontrolled glaucoma
- •Patients with history of bronchial asthma, thrombophlebitis, polyvalent allergy, cancer
- •Any intraocular surgery within 3 months in the study eye
- •Prior retinal or vitreous surgery including vitrectomy or scleral buckling
- •Any significant ocular disease other than AMD that has compromised or could compromise vision in the study eye and confound analysis of the primary outcome
- •Individuals with physical or mental disabilities that prevent accurate vision testing
- •History of any laser treatment of CNV in study eye (laser photocoagulation or prior photodynamic therapy), or anti-VEGF (ranibizumab or bevacizumab) in the past 2 years in the study eye.
结局指标
主要结局
Visual acuity
时间窗: Baseline and month 3
Best corrected visual acuity will be assessed by standardized vision testing, early treatment diabetic retinopathy study (ETDRS) test.
次要结局
未报告次要终点
研究者
Ekaterina Chikun
Researcher
Russian Academy of Medical Sciences