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Vistakon Investigational Contact Lenses Worn for Daily Wear

NCT00717249 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 529

Last updated 2016-05-26

Study results available
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Summary

This study compares the performance of an investigational contact lens to a currently marketed lens.

Conditions

  • Myopia

Interventions

DEVICE

galyifilcon A control lens

Marketed daily wear contact lens

DEVICE

galyfilcon A with a silver additive

Investigational daily wear contact lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2008-04-30
Completion
2008-04-30

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 NCT00717249 on ClinicalTrials.gov