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The Effect of Silicone Hydrogel Contact Lenses on Conjunctival Flora

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00531375
Enrollment
60
Registered
2007-09-18
Start date
2007-09-30
Completion date
2008-09-30
Last updated
2008-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia

Brief 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.

Interventions

Sponsors

Clinical Vision Research Australia
CollaboratorOTHER
Johnson & Johnson Vision Care, Inc.
CollaboratorINDUSTRY
University of Melbourne
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Is correctable to at least 6/9 distance visual acuity in each eye with spherical contact lenses. * Is a current full time soft contact lens wearer. * Has no clinically significant anterior eye findings. * Has no other active ocular disease

Exclusion criteria

* Has any systemic disease that might interfere with contact lens wear * Is using any systemic or topical medications that will affect ocular health. * Has any pre-existing ocular irritation that would preclude contact lens fitting. * Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses. * Has undergone corneal refractive surgery. * Is pregnant, lactating or planning a pregnancy. * Is participating in a concurrent clinical trial. * Has a latex sensitivity.

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026