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临床试验/JPRN-jRCT2032210430
JPRN-jRCT2032210430
已完成
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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2021年11月19日

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
myopia,myopia astigmatism
发起方
Ishibashi Taro
入组人数
104
状态
已完成
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2021年11月19日
结束日期
待定
最后更新
2年前
研究类型
Interventional
性别
All

研究者

发起方
Ishibashi Taro

入排标准

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

结局指标

主要结局

未指定

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