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A Comparison of Visual Function After Bilateral Implantation of Presbyopia-Correcting Intraocular Lenses (IOLs)

NCT01257217 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2018-07-02

Study results available
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Summary

The purpose of this study is to evaluate visual and refractive parameters in a series of subjects bilaterally implanted with presbyopia-correcting intraocular lenses (IOLs) during cataract surgery.

Conditions

  • Cataract

Interventions

DEVICE

AcrySof® IQ ReSTOR® +3.0 D Multifocal IOL Model SN6AD1

Multifocal IOL implanted for long-term use over the lifetime of the cataract patient

DEVICE

AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric IOL Model SND1TT

Multifocal IOL with extended secondary focal point and astigmatism correction implanted for long-term use over the lifetime of the cataract patient

DEVICE

Acri.LISA® 366D IOL

Aspheric diffractive IOL with +3.75 D add power implanted for long-term use over the lifetime of the cataract patient

DEVICE

Acri.LISA® 466TD Toric IOL

Aspheric diffractive IOL with +3.75 D add power and astigmatism correction implanted for long-term use over the lifetime of the cataract patient

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Brand Lead, Surgical, Global Medical Affairs · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-11-30
Primary Completion
2011-06-30
Completion
2011-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01257217 on ClinicalTrials.gov