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
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