Status:
COMPLETED
Effects of Contact Lens Care Regimens on the Corneal Epithelium
Lead Sponsor:
University of Waterloo
Collaborating Sponsors:
Alcon Research
Conditions:
Myopia
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare the performance of two different contact lens care solutions, specifically their affects on the front surface of the eye.
Eligibility Criteria
Inclusion
- Is at least 18 years old and has full legal capacity to volunteer.
- Has read, understood and signed an Information Consent Letter.
- Is willing and able to follow instructions and maintain the appointment schedule.
- Is correctable to a visual acuity of 6/6 or better (each eye), with their habitual visual correction.
- Has normal binocular vision (no strabismus, no amblyopia, and anisometropia less than or equal to 1.00 D).
- Has clear corneas and no active ocular disease.
- Has had an ocular examination in the last 2 years.
- Has not worn contact lenses before, or has worn contact lenses only for a trial period, with no trials occurring within the last six months.
- An ineligible contact lens wearer is one who:
- Responds positively to points 1 to 7 above.
- Has a distance contact lens prescription between -0.50D and -9.00 D.
- Has astigmatism less than or equal to -1.00D cyl.
- Currently wears silicone hydrogel contact lenses successfully.
- Agrees to wear the study lenses on a daily wear basis without the use of ocular or lens lubricants.
Exclusion
- Has undergone corneal refractive surgery.
- Is aphakic.
- Has any active ocular disease.
- Has any systemic disease affecting ocular health.
- Is using any systemic or topical medications that may affect ocular health.
- Has known sensitivity to the diagnostic pharmaceuticals to be used in the study.
- Is pregnant or lactating.
- Is participating in any other type of clinical or research study.
- An ineligible contact lens wearer is one who:
- Responds positively to any of points 1 to 8 above for exclusion criteria.
- Has known sensitivity to the contact lens care solutions used in the study.
- Has ocular or systemic allergies that could adversely affect contact lens wear.
- Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses.
- Has pinguecula/pterygium that in the investigator's judgement makes contact lens wear inadvisable.
Key Trial Info
Start Date :
June 1 2005
Trial Type :
INTERVENTIONAL
End Date :
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00349882
Start Date
June 1 2005
Last Update
July 10 2006
Active Locations (1)
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1
Centre for Contact Lens Research, University of Waterloo
Waterloo, Ontario, Canada, N2L 3G1