Clinical Performance of Extended Wear Silicone Hydrogel Lenses

Not Applicable

Completed

• Conditions: Myopia

• Registration Number: NCT00441233
• Lead Sponsor: University of Melbourne

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2007-02-27
• Study First Submitted QC: 2007-02-27
• Study First Posted: 2007-02-28
• Study Start: 2007-03
• Primary Completion: 2007-11
• Status Verified: 2007-12
• Study Completion: 2007-12
• Last Update Submitted: 2007-12-27
• Last Update Posted: 2008-01-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Trial Locations

Locations (1)

Clinical Vision Research Australia; 🇦🇺 Melbourne, Victoria, Australia