A-constant Optimization of a Toric Monofocal IOL

Status Completed

Clinical Trial Summary

The study is a prospective series study to determine the IOL constant of a hydrophilic toric monofocal intra-ocular lens (IOL)

Clinical Trial Description

The study is a prospective series study with he principal objective to determine the IOL constant. The secondary objectives of this study are to determine the rotational stability of the Ankoris intraocular lens and to measure the residual astigmatism after Ankoris IOL implantation with respect to the targeted astigmatism correction. Although there may be no direct benefit to the subjects under study, the investigation will determined the optimized constant for accurate IOL power calculation and will assess the stability and efficacy of the toric optics: this would result in a benefit for the patient population. Since the material, the overall design of the IOL as well as the measuring procedure in this study is well tolerated in standard clinical practice and the IOL is readily available and CE-marked, the benefit/risk ratio appears acceptable. ;

Study Design

Related Conditions & MeSH terms

Cataract

Clinical Trial Details

NCT number	NCT04944238
Study type	Observational
Source	Beaver-Visitec International, Inc.
Contact
Status	Completed
Phase
Start date	November 3, 2014
Completion date	June 11, 2019

View Details

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