跳至主要内容
临床试验/DRKS00015316
DRKS00015316已完成4 期

Refractive Accuracy and Rotational stability with an Aspheric Toric Intraocular Lens With and Without Implantation of a Capsular Tension Ring - a randomized two parallel arms clinical trial - - tIOL / CTR Studie

OcuNet GmbH & Co KG0 个研究点目标入组 179 人开始时间: 2018年8月27日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
179

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • intended implantation of Tecnis Toric in one or both eyes - age-related cataract with regular astigmatism - requiring an IOL power between 16.0 and 26.0 D SEQ - intended and reasonable ambulant cataract surgery -age 18 and older - regular astigmatism with a corneal cylinder between 0.75 and -2.75 D - patients with a post-operative potential best-corrected visual acuity of 0.5 or better based on the estimation of the surgeon - written informed consent to surgery, participation in the study and data protection

排除标准

  • - the partner eye was already recruited - relevant concomitant ophthalmic diseases (such as significant cornea guttata, significant corneal scar/opacity, glaucoma, NPDR stage II or II, PDR, pseudoexfoliation, trauma, AMD and other co-morbidity that could result in an outcome worse than UCVA 0.5 or that might affect capsular bag stability) - history of relevant previous ocular surgery (such as corneal surgery, glaucoma surgery, vitreoretinal surgery, other surgery) which might result in an outcome worse than UCVA 0.5 or that might affect capsular stability - expected residual cylinder = 0,5 dpt - Patient participates in other clinical trials

研究者

发起方
OcuNet GmbH & Co KG

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