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临床试验/JPRN-jRCT2032210430
JPRN-jRCT2032210430已完成未知

Multicenter study of lens posterior chamber lenses in patients with moderate to degree myopia or myopia astigmatism-efficacy and safety verification test on ATW001

Ishibashi Taro0 个研究点目标入组 104 人开始时间: 2021年11月19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
104

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
>= 18age old 至 <= 45age old(—)
性别
All

入选标准

  • Cases in which written consent was obtained from the patient himself / herself
  • Cases in which prescribed postoperative examinations may be possible during the study period
  • Cases where he/she can understand the contents of the consent explanation document and sign the consent form

排除标准

  • Cases of active external ocular inflammation
  • Cases with cataract nuclear myopia
  • Not limited to nuclear cataracts, but also includes cases with abnormalities such as opacity or subluxation of the crystalline lens.
  • Cases with active endoocular inflammation associated with uveitis or scleritis
  • Cases with high intraocular pressure
  • Cases with systemic or immunodeficiency disorders that are likely to affect wound care, such as severe diabetes and severe atopic dermatitis
  • Cases which are pregnant or breastfeeding
  • Cases with superficial anterior chamber and corneal endothelial cell damage
  • Cases of glaucoma whose treatment cannot be controlled by drugs, etc.
  • Cases with systemic connective tissue disease
  • Cases with suspected or history of macular degeneration or macular edem
  • Cases with amblyopia or blindness in one eye
  • Cases with progressive lesions that affect vision excludes retinal lesions associated with myopia
  • Cases with ocular surface disease
  • Cases judged by the investigator to be inappropriate as subjects

研究者

发起方
Ishibashi Taro

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