Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4

Alcon Research17 enrolled

Overview

Determine the clinical visual outcomes following bilateral implantation of the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) and to demonstrate what percentage of the subjects obtain spectacle freedom.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Cataract

Interventions

AcrySof ReSTOR Aspheric +4DEVICE

Implantation with the AcrySof ReSTOR Aspheric +4 Multifocal Intraocular Lens (IOL)

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosed with cataracts Exclusion Criteria: * Preexisting conditions confounding results; \> 1 Diopter preoperative astigmatism

Locations (1)

Contact Alcon Call Center for Trial Locations

Fort Worth, Texas, United States

Outcomes

Primary Outcomes

Visual Acuity

Time frame: 6 months

Secondary Outcomes

Contrast sensitivity, patient survey

Time frame: 6 months

Data from ClinicalTrials.gov

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