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Posterior Capsule Opafication of Two Different Hydrophobic Acrylic Intraocular Lenses — Acryvivi  

Age Related Cataracts Clinical Trial

Official title:
Posterior Capsule Opafication of Two Different Hydrophobic Acrylic Intraocular Lenses: Vivinex iSert P261 vs. Acrysof SN60WF

Clinical Trial Summary

On the day of surgery, the first eye to be operated is randomised to receive a Vivinex , HOYA Surgical Optics GmbH or an SN60WF, Alcon, Fort Worth, Texas. The second eye to be operated receives the other IOL type.

A complete biomicroscopic examination, visual acuity testing using autorefractometer, contrast sensitivity testing, and standardised retroillumination photography for PCO evaluation, will be performed 6 month (30-60 days), 1.5 years (± 3 months) and 3 (± 3 months) years postoperatively.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04196673
Study type Interventional
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date September 1, 2015
Completion date August 23, 2019
View Details
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