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Clinical Evaluation of the Long-Term Effects of Contact Lens Care Systems

NCT00813761 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 473

Last updated 2018-06-19

Study results available
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Summary

The purpose of this study is to compare two marketed contact lens care solutions in regards to comfort and ocular health.

Conditions

  • Myopia

Interventions

DEVICE

O2Optix contact lens

control contact lens to be worn daily for approximately 7 months for entire length of study.

DEVICE

Proclear contact lens

control contact lens to be worn for entire length of study.

DEVICE

ReNu MultiPlus Multi-Purpose Solution

lens solution for overnight lens disinfection

DEVICE

Clear Care Cleaning and Disinfecting Solution

lens solution for overnight lens disinfection

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-09-01
Primary Completion
2009-08-01
Completion
2009-08-01

Countries

  • United States
  • United Kingdom

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 NCT00813761 on ClinicalTrials.gov