Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3

Alcon Research1 个研究点分布在 1 个国家目标入组 218 人2007年9月

适应症Cataract

概览

阶段: 4 期
干预措施: 未指定
疾病 / 适应症: Cataract
发起方: Alcon Research
入组人数: 218
试验地点: 1
主要终点: Uncorrected Visual Acuity (UCVA)
状态: 已完成
最后更新: 16年前

概览研究者入排标准结局指标研究点相似试验

概览

简要总结

A prospective evaluation of the visual parameters in a series of patients bilaterally implanted with AcrySof ReSTOR +3 Intraocular Lens (IOL).

注册库

clinicaltrials.gov

开始日期

2007年9月

结束日期

2009年5月

最后更新

16年前

研究类型

Interventional

研究设计

Single Group

性别

All

研究者

发起方

Alcon Research

入排标准

入选标准

•Diagnosed with cataracts

排除标准

•Pre-existing conditions that could skew the results or are contraindications for the ReSTOR intraocular lens;
•\<1 diopter astigmatism by keratometry readings.

结局指标

主要结局

Uncorrected Visual Acuity (UCVA)

时间窗: 6 months

Uncorrected Visual Acuity (UCVA) measured by means of logMAR at various distances (40 centimeters (cm), 50 cm, 60 cm, 70 cm, and 4 meters (m)). Visual Acuity (VA) is measured in logMAR. LogMAR is the "logarithm of the minimum angle of resolution". A lower logMAR value indicates better visual acuity.