Status:
COMPLETED
Evaluation of an Investigational Multi-Purpose Disinfecting Solution for the Care of Silicone Hydrogel Soft Contact Lenses
Lead Sponsor:
Alcon Research
Conditions:
Contact Lens Care
Eligibility:
All Genders
Phase:
NA
Brief Summary
The objective of the study was to clinically evaluate the safety and effectiveness of a new multi-purpose disinfecting solution in patients wearing silicone hydrogel soft contact lenses.
Eligibility Criteria
Inclusion
- Successful daily wear of Night \& Day® or Acuvue® Advance™ silicone hydrogel contact for at least two weeks.
- Use of AOSEPT® ClearCare™ only as the pre-study care regimen for at least two weeks (rewetting drops use is also acceptable).
- Successful lens wear for at least 8 hours per day.
- Vision correctable to 20/30.
- Normal eyes - no current ocular abnormalities that prevent successful contact lens wear.
- No corneal surgery within the past 12 months.
- No systemic disease that affects that eye or that could be worsened by the use of contact lenses or solutions.
- No over-the-counter or prescription ocular medication.
- No enrollment in another clinical study within 30 days prior to enrollment.
Exclusion
Key Trial Info
Start Date :
August 1 2004
Trial Type :
INTERVENTIONAL
End Date :
February 1 2005
Estimated Enrollment :
233 Patients enrolled
Trial Details
Trial ID
NCT00382902
Start Date
August 1 2004
End Date
February 1 2005
Last Update
August 16 2012
Active Locations (1)
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1
Portland Site
Portland, Maine, United States, 04101