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临床试验/NL-OMON52343
NL-OMON52343招募中不适用

MyopiaX Treatment for the Reduction of Myopia Progression in Children and Adolescents: Safety and Efficacy Investigation - MyopiaX-1

Dopavision GmbH0 个研究点目标入组 10 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
10

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
2 至 15(—)

入选标准

  • - Myopic children (-0.75 to -5.0 D SER, least myopic meridian -0.50 D in each
  • - At least VA 0.2 LogMAR in each eye
  • - Age: 6 - 12 years old
  • - Good tolerability of test session with VR system
  • - Binocular adequacy as tested with VR
  • - Ability to understand treatment and give valid assent

排除标准

  • - Concomitant or previous therapies for myopia
  • -Eye diseases/conditions:
  • - Anisometropia >= 1.5 D
  • - Astigmatism >= 3 D
  • - Ophthalmological comorbidities
  • - Optic nerve abnormalities
  • - Suspicion of syndromic or monogenetic myopia
  • - Systemic illnesses affecting eye health, eye growth, and/or refraction
  • - Any illnesses affecting dopamine function (e.g., sleep
  • disorder, ADHD, Parkinson Disease, and autism spectrum
  • - Medication affecting dopamine function, accommodation, pupil size, or having
  • an impact on the ocular surface (topical ocular medications)
  • - Participation in other clinical studies
  • - Medical history (or family history) of photosensitive epilepsy

研究者

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