MedTrace Logo

Evaluation of the Aspheric ReSTOR Intraocular Lens (IOL) After Routine Cataract Extraction

NCT00565695 · 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 IOL.

Conditions

  • Cataract Extraction
  • Refractive Surgery

Interventions

DEVICE

aspheric ReSTOR multifocal intraocular lens (IOL)

Multifocal intraocular lens

Sponsors & Collaborators

  • Medical University of South Carolina

    lead OTHER

Principal Investigators

  • Kerry D Solomon, MD · Medical University of South Carolina, Storm Eye Institute

Eligibility

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

Timeline & Regulatory

Start
2007-10-31
Completion
2008-09-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00565695 on ClinicalTrials.gov