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Trials / Completed

CompletedNCT00758576

ReSTOR Natural +3.0D Study In Japan

ReSTOR Natural +3.0D (Diopter) Study In Japan

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

Summary

The objective of this study is to evaluate safety and effectiveness of ACRYSOF Multifocal Single-piece Intraocular Lens (IOL) Model SN6AD1 when implanted to replace the natural lens following cataract removal.

Conditions

Interventions

TypeNameDescription
DEVICEACRYSOF Multifocal Single-piece Intraocular Lens (IOL) Model SN6AD1Implantation with the AcrySof ReSTOR Intraocular Lens (IOL) Model SN6AD1 following cataract removal.

Timeline

Start date
2008-02-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2008-09-25
Last updated
2010-12-21
Results posted
2010-12-02

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT00758576. Inclusion in this directory is not an endorsement.

ReSTOR Natural +3.0D Study In Japan (NCT00758576) · Clinical Trials Directory