Clinical Performance of Extended Wear Silicone Hydrogel Lenses

University of Melbourne1 site in 1 countryMarch 2007

ConditionsMyopia

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Myopia
Sponsor: University of Melbourne
Locations: 1
Status: Completed
Last Updated: 18 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens over a period of 6 months of extended wear.

Registry

clinicaltrials.gov

Start Date

March 2007

End Date

December 2007

Last Updated

18 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

University of Melbourne

Eligibility Criteria

Inclusion Criteria

•Is correctable to at least 6/9 distance visual acuity in each eye with spherical contact lenses.
•Is a current daily wear 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.