Clinical Trials Directory

Trials / Completed

CompletedNCT01061918

Evaluation Of Bilateral Tecnis Multifocal Versus ReSTOR 3D Intraocular Lenses

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Innovative Medical · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the visual outcomes with bilateral implantation of Tecnis MF and ReSTOR intraocular lenses (IOLs) 6 months post cataract surgery.

Conditions

Interventions

TypeNameDescription
DEVICETecnis MF20 patients in the Tecnis MF group.
DEVICEReSTOR20 patients in the ReSTOR group.

Timeline

Start date
2009-08-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2010-02-03
Last updated
2011-02-17

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01061918. Inclusion in this directory is not an endorsement.