A Prospective Study of Two Daily Disposable Contact Lenses
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | Any |
Updated: | 10/21/2012 |
Start Date: | July 2012 |
End Date: | September 2012 |
Contact: | Alcon Call Center |
Phone: | 1-888-451-3937 |
The purpose of this study is to evaluate the performance of two daily disposable contact
lenses in subjects with contact lens-related dryness symptoms.
Inclusion Criteria:
- Be of legal age of consent and sign written Informed Consent Document and HIPAA form.
- Currently wearing soft contact lenses and identified as having contact lens-related
dryness symptoms based upon responses to the Contact Lens Dry Eye Questionnaire.
- Wearing either daily disposable contact lenses or bi-weekly/monthly replacement
contact lenses, daily wear use only (no extended wear use).
- Able to achieve distance visual acuity of at least 20/25 in each eye with study
lenses in the available parameters, -0.50D to -6.00D.
- Willing to wear study lenses for at least 8 hours/day and at least 5 days/week.
- Willing and able to follow instructions and maintain the appointment schedule.
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
- Neophyte or current wearer of DAILIES TOTAL1® or 1-DAY ACUVUE® MOIST™ contact lenses.
- Requires monovision or presbyopic correction.
- Any systemic or ocular disease or disorder complicating factors or structural
abnormality that would negatively affect the conduct or outcome of the study.
- Recent (within 7 days of enrollment) or current ocular infection, active ocular
inflammation, glaucoma or preauricular lymphadenopathy.
- Clinically significant lash or lid abnormality.
- Systemic disease that, in the investigator's best judgment, would prohibit or
confound safe contact lens wear.
- History of ocular surgery/trauma within the last 6 months.
- Topical or systemic antibiotics use within 7 days of enrollment.
- Other protocol-defined exclusion criteria may apply.
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