Clinical Trials Directory

Trials / Completed

CompletedNCT00759096

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.

Conditions

Interventions

TypeNameDescription
DEVICERESTOR IOL Model SA60D3Implanted into the study eye following cataract extraction surgery

Timeline

Start date
2007-05-01
Primary completion
2008-07-01
Completion
2008-07-01
First posted
2008-09-25
Last updated
2023-12-05
Results posted
2010-02-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00759096. Inclusion in this directory is not an endorsement.