Clinical Trials Directory

Trials / Completed

CompletedNCT01605877

AcrySof® IQ ReSTOR® +2.5 D Multifocal Intraocular Lens (IOL) Model SN6AD2 [SV25T0] in Japan

Clinical Investigation of AcrySof® IQ ReSTOR® Multifocal Intraocular Lens Model SN6AD2

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

Summary

The purpose of this study is to evaluate safety and effectiveness of AcrySof® IQ ReSTOR® +2.5 D Multifocal IOL Model SN6AD2 \[SV25T0\] in Japanese cataract patients.

Detailed description

Each subject completed a preoperative examination of both eyes, implantation of IOL at the operative visit for each eye, and up to 8 postoperative visits (each eye examined at Day 1-2, Day 7-14, and Day 30-60, with binocular visits at Day 120-180 and Day 330-420 after the second implantation). The second implantation occurred within 30 days of the first.

Conditions

Interventions

TypeNameDescription
DEVICEAcrySof® IQ ReSTOR® +2.5 D Multifocal IOL Model SN6AD2 [SV25T0]Multifocal IOL with extended secondary focal point implanted for long-term use over the lifetime of the cataract patient

Timeline

Start date
2012-05-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2012-05-25
Last updated
2015-07-07
Results posted
2015-06-09

Locations

2 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT01605877. Inclusion in this directory is not an endorsement.