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临床试验/CTRI/2023/03/050635
CTRI/2023/03/050635尚未招募3 期

Evaluation of visual, refractive outcome and changes in the ocular parameters after Eyecryl phakic IOL implementation in patients with moderate to high myopia and astigmatism: A prospective comparative study with EVO/EVO+ Visian implantable lenses

Prof MVanathi0 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
3 期
状态
尚未招募
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.Patients with myopic astigmatism within a spherical equivalent (SE) range of -3.00 to -20.00 D and a minimum astigmatism of -1.00 D, stable refraction (0.50 D or less change in the past 12 months),
  • 2.Minimum anterior chamber depth (ACD) from corneal endothelium of 2.8 mm,
  • 3.Endothelial cell count of 2,500 cells/mm2
  • 4.Absence of corneal ectatic diseases, corneal scars,
  • 5.Absence of retinal pathologies
  • 6.Patients willing to give written informed consent and attend all follow-up appointments

排除标准

  • 1.Subject with previous intraocular or corneal surgery
  • 2.Subject with ocular condition like any cataract of any grade, glaucoma, severe dry eye, herpetic keratitis, uveitis
  • 3.Subject with systemic conditions like diabetes, collagen vascular diseases, immunosuppression
  • 4.Subject who is Pregnant or planning to start family, or lactating during the course of the evaluation
  • 5.Other condition associated with fluctuation of hormones
  • 6.Monocular subject
  • 7.Patient not willing to give written informed consent and attend all follow-up appointments

研究者

发起方
Prof MVanathi

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