Two Daily Disposable Contact Lenses in Symptomatic Patients
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/5/2018 |
Start Date: | August 13, 2018 |
End Date: | September 25, 2018 |
The purpose of this study is to evaluate the performance of ACUVUE OASYS® 1-DAY and DAILIES
TOTAL1® with respect to visual acuity, dryness and discomfort in a symptomatic study
population of monthly or bi-weekly replacement lens wearers.
TOTAL1® with respect to visual acuity, dryness and discomfort in a symptomatic study
population of monthly or bi-weekly replacement lens wearers.
Inclusion Criteria:
- Able to understand and must sign an IRB-approved informed consent form;
- Soft contact lens wearers in both eyes during the past 3 months;
- Best-corrected visual acuity (BCVA) 20/25 or better in each eye;
- Willing to wear study lenses at least 3 days per week and at least 8 hours per day;
- Willing to stop wearing habitual contact lenses for the duration of study
participation;
- Other protocol-specified inclusion criteria may apply.
Exclusion Criteria:
- Infection, inflammation, abnormality, condition, disease, surgery, or use of
medications, as specified in the protocol;
- Intolerance, hypersensitivity, or allergy to any component of the study products;
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in
lenses for at least 1 night per week) over the last 3 months prior to enrollment;
- Monocular (only one eye with functional vision);
- Other protocol-specified exclusion criteria may apply.
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