Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
NCT ID: NCT00758940
Last Updated: 2015-05-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
PHASE4
INTERVENTIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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1
Acrysof ReSTOR multifocal IOL
Acrysof ReSTOR multifocal IOL
Implanted into the study eye following cataract extraction surgery
Interventions
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Acrysof ReSTOR multifocal IOL
Implanted into the study eye following cataract extraction surgery
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
21 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Alcon Research Ltd.
Locations
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Alcon Call Center
Fort Worth, Texas, United States
Countries
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Other Identifiers
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HK-Restor-YIU-01
Identifier Type: -
Identifier Source: org_study_id
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