A Study to Evaluate the Clinical Performance and Safety of UNICON Silicone Hydrogel Daily Disposable Soft Contact Lenses

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUnicon Optical Co. Ltd.

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

Treatment groups

35 Participants
are divided into 1 treatment group

Sponsors and collaborators