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Clinical Trial Summary

The study is an observational non-randomised controlled study comparing the visual acuity after implantation of the POD 26% FINEVISION TORIC with respect to the POD 26% TORIC


Clinical Trial Description

The study is an observational non-randomised controlled study comparing the visual acuity after implantation of the POD 26% FINEVISION TORIC with respect to the POD 26% TORIC This study includes both eyes of 24 patients implanted with the POD 26%FineVision Toric (group 1: 12 patients) and the POD 26% Toric (group 2: 12 patients) . The study primary goal is to compare the near visual acuity in both groups. Distance and intermediate visual acuities, defocus curve, refraction and straylight will be compared. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02426385
Study type Observational
Source Beaver-Visitec International, Inc.
Contact
Status Withdrawn
Phase
Start date April 2015
Completion date October 2015

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