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临床试验/CTRI/2016/02/006636
CTRI/2016/02/006636尚未招募4 期

â??Post Marketing, Non-Randomized Open label Single Arm, Prospective study to evaluate the clinical outcomes in patients implanted with a foldable, hydrophobic acrylic, natural yellow, single piece, injectable, Toric Intraocular Lens - toric iol

ethradhama super speciality eye hospital0 个研究点目标入组 40 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
40

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

  • Unilateral/Bilateral cataract
  • Patient must have preoperative regular corneal astigmatism from 0.75 to 2.50 D as per corneal topography or keratometry
  • Patients who have and will attend all follow-up appointments
  • Patients must sign and be given a copy of the written Informed Consent form

排除标准

  • Preoperative ocular pathology
  • Presence of irregular corneal astigmatism
  • Ocular co-morbidities affecting visual outcomePrevious intra ocular or corneal surgery
  • Corneal Opacities
  • Ophthalmic diseases such as pseudoexfoliation, glaucoma, traumatic cataract corneal scars and other co-morbidity that could affect capsule bag stability
  • Pre-existing corneal astigmatism lesser than 0.75 D Pre-existing retinal disease

研究者

发起方
ethradhama super speciality eye hospital

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