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Clinical Trials/NCT01253239
NCT01253239
Completed
Not Applicable

A Retrospective Evaluation Comparing Post Operative Visual Outcomes in Patients Implanted With the TECNIS IOL in Both Eyes Versus the ReZoom IOL in One Eye and TECNIS IOL in the Opposite Eye

Frank A. Bucci, Jr., M.D.1 site in 1 country175 target enrollmentNovember 2010
ConditionsCataract

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
Frank A. Bucci, Jr., M.D.
Enrollment
175
Locations
1
Primary Endpoint
Uncorrected visual acuity at distance and near
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the visual performance of two cohorts of patients who received multifocal intraocular lenses following cataract and clear lens extraction surgeries. Comparing visual outcomes of patients who were implanted with TECNIS Multifocal IOLs in both eyes versus patients implanted with TECNIS Multifocal in one eye and ReZoom Multifocal IOL in the opposite eye.

Detailed Description

Stable post operative cataract and clear lens extraction patients who have been implanted with either the TECNIS Multifocal IOL in both eyes or TECNIS Multifocal IOL in one eye and theReZoom Multifocal IOL in the opposite eye. Study Design-A retrospective chart review to collect visual outcomes to determine lens performance. Patient satisfaction questionnaire will be administered to determine spectacle independence.

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
July 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Frank A. Bucci, Jr., M.D.

Principal Investigator

Bucci Laser Vision Institute

Eligibility Criteria

Inclusion Criteria

  • Patients who have undergone surgery and received either the TECNIS Multifocal Intraocular lens in one eye and the ReZoom Multifocal Intraocular lens in the other will be evaluated. Males and Females with ages ranging from 42 years to 86 years old.

Exclusion Criteria

  • Patients who have subsequently developed any visual limiting problems (e.g. corneal, retinal, infection) which could potentially limit their post operative visual potential.

Outcomes

Primary Outcomes

Uncorrected visual acuity at distance and near

Time Frame: Six months

Secondary Outcomes

  • Patients Satisfaction(Six months)

Study Sites (1)

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