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临床试验/NCT01464710
NCT01464710已完成不适用

Genetic Assessment of Early to Late macuLar dEgeneration studY 2

Henry Ferreyra3 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2008年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
170
试验地点
3
主要终点
To determine the allele frequency for patients that progress to bilateral advanced AMD in the study eye

研究概览

简要总结

The purpose of this study is to determine if polymorphisms at rs11200638 on HTRA1 and rs1061170 on CFH are associated with an accelerated progression to advanced AMD (wet AMD or GA) in patients with early AMD (soft confluent drusen>120 microns ) in the study eye, and with either early AMD or advanced AMD in the non-study eye.

详细描述

Age-related macular degeneration (AMD) is the leading cause of blindness in the developed world. To date, two major polymorphisms on the HTRA1 and CFH genes have been associated with AMD. Progression and vision loss need to be followed and treated promptly in order to preserve vision. This study will provide more information on the genetics of disease progression and may lead to future guidelines for patient follow-up and treatment.

This study consists of a blood draw and observation of eye conditions. Consented, enrolled patients will come in every four months as per standard of care. At each visit, visual acuity measurement, slit lamp exam, indirect ophthalmoscopy, fundus photos, and spectral domain optical coherence tomography will be performed. Every 8 months, or per standard of care, fluoroscein angiography will be performed. DNA extraction and genotyping will be performed, and correlations between HTRA1 and CFH genotypes and the progression to bilateral advanced AMD will be analyzed.

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

  • Subjects will be eligible if the following criteria are met:
  • Ability to provide written informed consent and comply with study assessments for the full duration of the study
  • Age > 45 years
  • Disease related considerations
  • Subjects with a diagnosis of advanced AMD in one eye (either CNV or geographic atrophy) and soft confluent drusen in the study eye OR subjects with bilateral large soft drusen.

排除标准

  • Subjects with any other progressive retinal disease that may impair the physician's ability to assess the severity of AMD

结局指标

主要结局

To determine the allele frequency for patients that progress to bilateral advanced AMD in the study eye

时间窗: 5 years

次要结局

  • To determine the allele frequency for patients that do not progress to bilateral advanced AMD in the study eye.(5 years)

研究者

发起方
Henry Ferreyra
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Henry Ferreyra

Principal Investigator

University of California, San Diego

研究点 (3)

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