Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Alcon Research
This single visit study is designed to help understand how vision is affected if the eye still has astigmatism after cataract surgery. Participants will be individuals who have already undergone cataract surgery and received a Clareon Vivity IOL in both eyes at least 4 months prior to study enrollment. During the study visit, trial lenses (glass lenses that are used during an eye exam) will be used to temporarily create the effect of astigmatism on the eye.
Age
22–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Able to understand and sign an Institution Review Board-approved informed consent form;
Willing and able to attend all scheduled study visits as required by the protocol;
Implanted with study IOLs in both eyes at least 4 months prior to study participation;
Best Corrected Distance Visual Acuity (BCDVA) of 0 logarithm minimum angle of resolution (logMAR) or better in each eye.
You may not be if
Residual astigmatism greater than or equal to 1.00 diopter (D);
Clinically significant ocular conditions as specified in the protocol;
History of ocular surgeries other than limbal relaxing incisions
Clareo Health | Visual Performance With Clareon® Vivity® Intraocular Lenses (IOLs)
