Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Alcon Research
Subjects will wear two products and be expected to attend 4 office visits. The individual duration of participation will be approximately 65 days, which includes approximately 30 days of exposure to the test product and approximately 30 days of exposure to the comparator product.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Able to understand and sign an approved Informed Consent form;
Willing and able to attend all scheduled study visits as required by the protocol;
Currently wearing any commercial spherical weekly/monthly soft contact lenses in both eyes for at least 3 months, minimum 5 days per week, 10 hours per day;
Manifest cylinder less than or equal to 0.75 diopter (D) in each eye;
Willing to stop wearing habitual contact lenses for the duration of study participation.
You may not be if
Any eye condition that contraindicates contact lens wear, as determined by the Investigator;
Any use of systemic or ocular medicine that contraindicates contact lens wear, as determined by the Investigator;
Ocular or intraocular surgery (excluding placement of punctal plugs) within the previous 12 months or planned during the study;
Any use of topical ocular medications and artificial tear or rewetting drops that would require instillation during contact lens wear;
Current or prior Biofinity contact lens wear in the past 3 months prior to consent.
