Contralateral ReSTOR / Monofocal or Phakic Eye

NCT00731640 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2010-03-23

Study results available
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Summary

Bilateral evaluation of unilateral implantation of ReSTOR and contralateral monofocal or phakic eye.

Conditions

  • Cataracts

Interventions

DEVICE

ReSTOR

AcrySof ReSTOR +4 Intraocular Lens (IOL) unilaterally implanted

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2008-05-31

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 NCT00731640 on ClinicalTrials.gov