Protocol for Comparison of ocular biometry measurements in NOA and IOLMaster 500. - NI

Elisar Vision Technology0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年4月29日

试验速览

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•1. Visual acuity as tested within one week of the trial should be better than 6/18 will be selected for the study.
•2. One eye of each patient should be selected by either randomly or the eye operated first.
•Inclusion for Controls
•1. Patients said to be clinically normal by ophthalmologist.
•Inclusion for Cataract
•1. Patients diagnosed with cataract graded using the LOCS grading method by ophthalmologist.
•2. Eyes that are undergoing cataract surgery candidates in the clinic

•1. Presence of keratoconus or suspect keratoconus, a previous diagnosis of dry eye, history of any corneal disease or trauma, any kind of ocular surgery, and use of contact lens past month.
•2. Eyes with retinopathy or maculopathy, eyes with a history of corneal disease, pseudophakic eyes.
•3. Patients with corneal pathology, previous refractive surgery or abnormalities in the anterior segment.

发起方

Elisar Vision Technology