Status:
UNKNOWN
Evaluation of Corneal Staining With Various Contact Lens/Solution Combinations
Lead Sponsor:
Andrasko, Gary, OD, LLC
Collaborating Sponsors:
Alcon Research
Conditions:
Corneal Epithelial Disruption
Corneal Staining
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to quantify the amount of corneal staining observed with various marketed contact lens/multipurpose solution combinations. The hypothesis is that there are measurable diff...
Detailed Description
A series of clinical studies is being conducted at one research site using a double-masked, randomized cross-over design. Each study consists of asymptomatic daily wear soft contact lens wearers obser...
Eligibility Criteria
Inclusion
- currently wearing soft contact lenses daily wear for at least 2 weeks prior to study
- correct visual acuity of 20/30 or better each eye
Exclusion
- history of hypersensitivity to any components of solution being tested
- any ocular condition prohibiting contact lens wear
- excessive baseline staining as defined in protocol
- use of topical or OTC ocular medications during the study
- seasonal allergies with significant effect on contact lens wear
Key Trial Info
Start Date :
July 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2008
Estimated Enrollment :
200 Patients enrolled
Trial Details
Trial ID
NCT00381446
Start Date
July 1 2005
End Date
March 1 2008
Last Update
September 27 2007
Active Locations (1)
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1
Dr. Richard Erdey office
Columbus, Ohio, United States, 43213