An Evaluation of Marketed Contact Lens Disinfectant Systems on Eyelid Tissues
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | Any |
Updated: | 2/4/2013 |
Start Date: | April 2012 |
End Date: | April 2013 |
Contact: | Alcon Call Center |
Phone: | 1-888-451-3937 |
The purpose of this study is to assess and compare the effect of two contact lens care
systems used in conjunction with hydrogel and silicone hydrogel contact lenses worn on a
daily wear basis for three months.
Inclusion Criteria:
- Successfully wearing a frequent replacement hydrogel or silicone hydrogel contact
lens brand under a frequent replacement (biweekly or monthly) daily wear modality;
- Classified as symptomatic according to protocol-specified criteria;
- Agree to wear study contact lenses as directed for the duration of the study;
- Best corrected visual acuity of 6/9 or better in each eye;
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
- Any known sensitivity or intolerance to any of the contact lenses or contact lens
care products to be used;
- Systemic disease or use of medication which might interfere with contact lens wear or
produce dry eye side effects;
- Ocular allergies or ocular disease which might interfere with contact lens wear or
data and information obtained in this study;
- Use of any concomitant topical ocular medications during the study period;
- Pregnant, planning to be become pregnant, or lactating at time of enrollment;
- Participation in an investigational drug or device study within 30 days of entering
study;
- Other protocol-defined exclusion criteria may apply.
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