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临床试验/CTRI/2023/03/050441
CTRI/2023/03/050441招募中Unknown

Efficacy of DIMS spectacle lenses among non-responders to 0.01% low dose Atropine.

HOYA Holdings0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方

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

入选标准

  • 1) Children with myopia of SE between -0.50 D and -10.00 D (combination of -6.00DS and -4.00 DC) of age group 6-12 years
  • 2) Documented history of myopia progression by more than - 0.50D and/or increase in axial length by more than 0.20mm between 6 months to one year while using 0.01% atropine once daily
  • 3) Corrected VA is = 0.1 Log MAR or 0.8 in Snellen.

排除标准

  • 1) Prior use of 0.01% low dose atropine twice a day
  • 2) History of any previous myopia control intervention other than 0.01% low dose atropine
  • 3) History of any ocular or systemic disease
  • 4) History of any previous ocular surgery or trauma
  • 5) Anisometropia > - 2.00 D; Astigmatism > - 1.50 D and Amblyopia
  • 6) Any hypersensitivity/allergic reaction with use of 0.01% atropine
  • 7) Myopia of higher than -8.00D (limited by availability of DIMS spectacle lens in power higher than that)

研究者

发起方
HOYA Holdings

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