About this trial
13 weeks, open-label, daily disposable contact lens dispensing study.
Eligibility criteria
Qualifiers
Adult with an age ≥ 18;
Be a currently adapted soft contact lens wearer who successful wear of soft contact lenses in both eyes for a minimum of 5 days per week and 6 hours per day within 3 months prior to study screening (by verbal confirmation);
Participant must be stop wearing any contact lenses more than 7 days prior to screening;
Able to wear contact lenses within a range of power from -2.00D to -6.00D (0.25 D steps) in both eyes;
Disqualifiers
Women who are currently pregnant;
Women who are lactating or planning a pregnancy at the time of enrollment (by verbal confirmation at the screening visit);
Any use of systemic or ocular medications (e.g., non-steroidal anti-inflammatory eye drops, ophthalmic steroids) within 30 days prior to study enrollment for which contact lens wear could be contraindicated, as determined by the investigator;
Any current or history ocular or systemic disease which may interfere with contact lens wear, as determined by the investigator;
Trial design
Treatments tested in this trial
- Treatment