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Four Week Performance Comparison Between Two Commercially Available Silicone Hydrogel Lenses

NCT01300767 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to compare the performance of two commercially marketed contact lenses when worn for up to 4 weeks in a daily wear modality.

Conditions

  • Myopia

Interventions

DEVICE

Lotrafilcon B contact lens (AIR OPTIX® AQUA)

Silicone hydrogel, single vision contact lens worn in one eye in a daily wear modality for approximately 5 days or more per week, at least 10 hours per day, for up to 4 weeks.

DEVICE

Balafilcon A contact lens (PureVision® 2)

Silicone hydrogel, single vision contact lens worn in one eye in a daily wear modality for approximately 5 days or more per week, at least 10 hours per day, for up to 4 weeks.

DEVICE

Contact lens solution (Clear Care®)

Hydrogen peroxide-based system used for cleaning, disinfection and overnight storage of the study contact lenses.

Sponsors & Collaborators

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2011-04-30
Completion
2011-04-30

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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 NCT01300767 on ClinicalTrials.gov