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Visual Function After Bilateral Implantation of AcrySof® Toric

NCT00758550 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2010-03-16

Study results available
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Summary

The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.

Conditions

  • Visual Function

Interventions

DEVICE

AcrySof® Toric IOL

AcrySof® Toric Intraocular Lens (IOL) implanted into the study eye following cataract extraction surgery

DEVICE

AcrySof Natural

AcrySof Natural Intraocular Lens (IOL) implanted into the study eye following cataract extraction surgery

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-04-30
Primary Completion
2008-06-30

Countries

  • United States

Study Locations

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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 NCT00758550 on ClinicalTrials.gov