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Evaluation of the Aspheric ReSTOR IOL After Routine Cataract Extraction

NCT00720005 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2010-10-04

No results posted yet for this study

Summary

The purpose of this study is to evaluate the visual outcomes and patient satisfaction after bilateral implantation of the aspheric ReSTOR multifocal intraocular lens (IOL) and compare it to a historical control group of patients implanted bilaterally with the spherical ReSTOR multifocal

Conditions

  • Cataract

Interventions

DEVICE

Aspheric Acrysof ReSTOR intraocular lens

Bilateral implantation of Aspheric Acrysof ReSTOR

Sponsors & Collaborators

  • Medical University of South Carolina

    lead OTHER

Principal Investigators

  • Kerry D. Solomon, MD · Assistant Professor

Eligibility

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

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-12-31
Completion
2008-12-31

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 NCT00720005 on ClinicalTrials.gov