Time Course Comparison of Contact Lens Maintenance Systems for Hydrogel Lenses
Not Applicable
Completed
- Conditions
- MyopiaHyperopia
- Interventions
- Device: Silicone Hydrogel Contact LensesDevice: 1x PMBH preserved MPSDevice: 1x Polyquad/Aldox MPS
- Registration Number
- NCT00732004
- Lead Sponsor
- University of Melbourne
- Brief Summary
The principal aim of this project is to determine the time course of development of contact lens and contact lens case contamination during daily wear of silicone hydrogel lenses. The secondary aim of the study is to determine whether the time course of development of contact lens and contact lens case contamination varies between two different contact lens care systems.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 132
Inclusion Criteria
- Distance contact lens prescription between +8.00 and -10.00D.
- Cylindrical component of refractive error no greater than 1.25D in either eye.
- Vision correctable to 6/12 (0.30 logMAR) or better in each eye.
- Healthy normal eyes without anterior segment infection, inflammation or abnormality, or significant slitlamp findings.
Exclusion Criteria
- Concurrent ocular medication
- Eye injury or surgery within twelve weeks immediately prior to enrolment.
- Current ocular irritation that would preclude contact lens fitting.
- Evidence of systemic or ocular abnormality, infection or disease likely to affect successful wear of contact lenses or use of their accessory solutions.
- Pregnant, lactating or planning a pregnancy.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1 Silicone Hydrogel Contact Lenses Group 1 2 1x PMBH preserved MPS Group 2 3 1x Polyquad/Aldox MPS Group 3
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Clinical Vision Research Australia
🇦🇺Melbourne, Victoria, Australia