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临床试验/ACTRN12619001109190
ACTRN12619001109190已完成未知

Investigation of AcrySof IQ Panoptix Presbyopia Correcting IOL for subjects with mild to moderate astigmatism

Alcon Laboratories0 个研究点目标入组 12 人开始时间: 2019年8月12日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
12

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
40 Years 至 o limit(—)
性别
All

入选标准

  • Subjects are eligible for the study if they meet the following criteria:
  • Note: Ocular criteria must be met in both eyes.
  • - are more than 40 years of age, of either gender and any race;
  • - have completed uncomplicated cataract surgery or refractive lens exchange surgery with the Alcon Panoptix Toric IOL at least 6 months prior (but no greater than 12 months)
  • - regular corneal astigmatism requiring toric IOL correction

排除标准

  • If any of the following exclusion criteria are applicable to the subject or either eye, the subject should not be enrolled in the study.
  • - Amblyopia
  • - Previous anterior or posterior chamber surgery (e.g., vitrectomy, laser iridotomy)
  • - Diabetic retinopathy
  • - Macular degeneration
  • - History of retinal detachment
  • - Subjects who have an acute or chronic disease or illness that would confound the results of this investigation (e.g., immunocompromised, connective tissue disease, clinically significant atopic disease, diabetes, and any other such disease or illness), that are known to affect post-operative visual acuity.

研究者

发起方
Alcon Laboratories

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