Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Tangible Science
With
University of Houston
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Habitual contact lens wear with a group 3 FDA approved rigid lens material, with 20-50% of subjects wearing corneal lenses
Willing and able to sign the informed consent form
18 years or older
You may not be if
Eye injury or surgery within the 3 months immediately prior to enrollment for this trial
Pre-existing ocular irritation that would preclude contact lens fitting
Current enrollment in an ophthalmic clinical trial
Evidence of systemic or ocular abnormality, infection, or disease which is likely to affect successful wear of contact lenses or use of the accessory solutions, as determined by the investigator
Any use of medications for which contact lens wear could be contraindicated, as determined by the investigator
Pregnant women and nursing mothers
Visual acuity less than 20/20 when best corrected with contact lenses
Clareo Health | Evaluation of Tangible Boost Replenishing System
