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The Effect of Silicone Hydrogel Contact Lenses on Conjunctival Flora

NCT00531375 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2008-11-19

No results posted yet for this study

Summary

The primary purpose of this study is to investigate the effect of silicone hydrogel contact lenses on conjunctival flora over a period of 6 months of daily wear. A secondary aim is to compare the levels of microbial contamination of silicone hydrogel lenses after daily wear.

Conditions

  • Myopia

Interventions

DEVICE

Silicone hydrogel contact lens

Sponsors & Collaborators

  • Clinical Vision Research Australia

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    collaborator INDUSTRY

  • University of Melbourne

    lead OTHER

Principal Investigators

  • Carol Lakkis, BScOptom, PhD, PGCertOcTher · Clinical Vision Research Australia, Victorian College of Optometry

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-06-30
Completion
2008-09-30

Countries

  • Australia

Study Locations

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Entities

Companies

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 NCT00531375 on ClinicalTrials.gov