Status:
COMPLETED
Subjective Comfort With Multipurpose and Hydrogen Peroxide Lens Care Solutions in Soft Contact Lens Wearers
Lead Sponsor:
Alcon Research
Conditions:
Contact Lens Wear
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study was to assess comfort in soft contact lens wearers.
Eligibility Criteria
Inclusion
- Wear silicone hydrogel contact lenses on a daily wear basis;
- Currently using OPTI-FREE RepleniSH contact lens solution;
- Report comfort above 75 on a Visual Analog Scale at the Baseline Visit;
- Read, sign, and date IRB-approved informed consent and the privacy document;
- Be generally healthy and have normal ocular health;
- Be be willing to follow the study procedures and visit schedule;
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Use of additional lens cleaners;
- Known sensitivity to any ingredient in either of the test articles;
- Systemic or ocular disease or disorder (except refractive error) that would negatively affect the conduct or outcome of the study;
- Prior (within 7 days of enrollment) or current ocular infections;
- Clinically significant lash or lid abnormality;
- History of ocular surgery/trauma within the last 6 months;
- Use of any topical ocular or systemic antibiotics or corticosteroids within 7 days of enrollment;
- Participation in any other ophthalmic drug or device clinical trial within 30 days of enrollment;
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
June 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT01164865
Start Date
June 1 2010
End Date
December 1 2010
Last Update
October 12 2012
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