Study Status: Completed
Recruit Status: Completed
Study Type: Observational [Patient Registry]
Official Title: Maximizing Visual Outcomes With Eyhance IOLs
Brief Summary: This is a non-interventional prospective, single center, bilateral, non-randomized, open-label, observational clinical study. All patients will have had bilateral implantation of an Eyhance IOL at the time of cataract surgery. These patients will then be compared to assess which patient biometric properties (such as spherical aberration, q value, pupil size, etc.) lead to an overall increase in near or intermediate vision as well as overall patient satisfaction.