Status:
COMPLETED
A Clinical Comparison of Three Contact Lens Care Systems and Their Effect on Contact Lenses
Lead Sponsor:
Alcon Research
Conditions:
Contact Lenses
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study was to evaluate the clinical performance of three differing contact lens care solutions when used in conjunction with three contact lenses.
Detailed Description
This study was conducted as three separate studies based on the contact lens brand dispensed. In each study, the contact lens was evaluated in conjunction with three solutions: Opti-Free Replenish, Re...
Eligibility Criteria
Inclusion
- Signed informed consent.
- Adapted contact lens wearer for at least one month.
- Spherical prescription range between +6.00 to -8.00 diopters.
- Astigmatism of less than or equal to 1.00 diopter in at least one eye.
- Normal eyes with no evidence of abnormality or disease.
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Rigid Gas Permeable (RGP) contact lens wear in last 30 days.
- Concurrent ocular medication, systemic illness, or medical treatment that will affect ocular physiology, lens performance, or vision.
- Corneal infiltrates, scarring, or neovascularization within central 4 millimeters of cornea.
- Eye injury or surgery within 8 weeks prior to study.
- Aphakia, amblyopia, abnormal lacrimal secretions, ocular irritation, keratoconus, corneal irregularity, pregnancy, lactating, planning to become pregnant during the study, and participation in a concurrent clinical trial.
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
April 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2010
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT00982046
Start Date
April 1 2009
End Date
May 1 2010
Last Update
November 16 2016
Active Locations (1)
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1
Visioncare Research Ltd.
Farnham, Surrey, United Kingdom, GU9 7EN