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临床试验/NL-OMON40755
NL-OMON40755已完成不适用

Influence of multifocal intraocular lens on glaucoma diagnostic tests - multifocal intraocular lens and glaucoma tests

niversitair Medisch Centrum Groningen0 个研究点目标入组 15 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
已完成
入组人数
15

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
18 至 99(—)

入选标准

  • - Patients implanted with a MFIOL aged between 18 an 70, who are able and willing to participate in this study.
  • - Postoperative period of at least 3 months.
  • - One eye will be randomly chosen and tested with the exception of the FDT. This device can only perform the test if both eyes are analysed.

排除标准

  • - Best correct visual acuity (BCVA) of <0.8 or <0.67 when aged above 50.
  • - Refractive error >±5D or a cylinder of >±2.5D.
  • - Intra ocular pressure (IOP) of >22mmHg.
  • - Optic nerve abnormalities indicating glaucoma
  • - Repeatable VF-defects detected with perimetry (not explained by the MFIOL in patients)
  • - History or current serious eye disease, trauma or surgery.

研究者

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