Phacoemulsification and Intraocular Lens Implantation: Patient Registry
Trial Parameters
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
Brief Summary
The aim of the study is to create a patient registry that will allow for comparison of cataract treatment outcomes using phacoemulsification with implantation of different types of intraocular lenses.
Eligibility Criteria
Inclusion Criteria: * Patients who have undergone cataract surgery or are scheduled for bilateral cataract surgery with implantation of an extended-depth-of-focus (EDOF) intraocular lens, a monofocal-plus intraocular lens, or a standard monofocal intraocular lens. Exclusion Criteria: * Anterior or posterior segment pathologies affecting postoperative visual acuity, including but not limited to: severe dry eye syndrome, corneal dystrophies, uveitis, retinal degenerative changes, glaucoma, or diabetic retinopathy. * Pseudoexfoliation syndrome * Keratoconus * History of laser refractive surgery * Prior ocular surgery other than cataract surgery * Amblyopia * Posterior capsule opacification * Postoperative best-corrected visual acuity (BCVA) less 0.5 * Intraoperative complications, including posterior capsule rupture