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Ophthalmic Compatibility During Seven Days of Continuous Wear of Silicone Hydrogel Lenses

NCT00934102 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 57

Last updated 2012-07-10

Study results available
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Summary

The purpose of this study is to assess the ophthalmic compatibility of three different silicone hydrogel lenses worn on an overnight basis for six nights.

Conditions

  • Myopia

Interventions

DEVICE

Narafilcon A contact lens

Investigational, silicone hydrogel, spherical soft contact lens

DEVICE

Lotrafilcon A contact lens

Commercially marketed, silicone hydrogel, spherical soft contact lens

DEVICE

Galyfilcon A contact lens

Commercially marketed, silicone hydrogel, spherical soft contact lens

Sponsors & Collaborators

  • University of Waterloo

    collaborator OTHER

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • Canada

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 NCT00934102 on ClinicalTrials.gov