Status:
COMPLETED
Clinical Performance of a Silicone Hydrogel Lens With Use of FID 114675A
Lead Sponsor:
Alcon Research
Conditions:
Contact Lens Fit
Myopia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate the clinical performance of a silicone hydrogel contact lens when used with an investigational multi-purpose disinfecting solution (MPDS).
Eligibility Criteria
Inclusion
- 18 years of age or older.
- History of at least 5 days successful daily wear (minimum 8 hours per day) of spherical, single power Acuvue® Advance® SiH contact lenses prior to Visit 1.
- Wear contact lenses a minimum of 8 hours per day prior to Visit 1.
- Vision correctable to 20/30 (Snellen) or better in each eye at distance with study lenses at Visit 1.
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Need to wear contact lenses on an extended wear basis (i.e., overnight) during the study.
- Use of products other than a multi-purpose solution to care for lenses at least 7 days prior to Visit 1. Pre-study use of rewetting drops is acceptable.
- History of intolerance or known sensitivity to any component of the treatments.
- Use of over-the-counter (OTC) or prescribed topical ocular medications within 7 days prior to Visit 1.
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
October 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2011
Estimated Enrollment :
89 Patients enrolled
Trial Details
Trial ID
NCT01240135
Start Date
October 1 2010
End Date
February 1 2011
Last Update
July 12 2012
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