Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00760058

Visual Outcome and Visual Quality After Bilateral Implantation of the AcrySof® IQ IOL Compared to MI60® and Tecnis® IOL

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

The objective of the study is to compare the visual outcomes of three aspheric monofocal intraocular lenses after cataract surgery - ACRYSOF® IQ, Tecnis® and Akreos® MI60.

Conditions

Interventions

TypeNameDescription
DEVICEAcrySof® IQ IOLReplacement of natural crystalline lens in cataract surgery
DEVICETecnis® Aspheric intraocular lensReplacement of natural crystalline lens in cataract surgery
DEVICEAkreos® MI60 intraocular lensReplacement of natural crystalline lens in cataract surgery

Timeline

Start date
2008-06-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2008-09-25
Last updated
2015-05-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00760058. Inclusion in this directory is not an endorsement.