About this trial
To investigate the patient Quality of Life and satisfaction outcomes of combined cataract surgery with retinal surgery for visually significant epiretinal membrane in patients receiving Vivity IOL versus standard monofocal controls.
Eligibility criteria
Qualifiers
Adult patients with visually significant epiretinal membrane who are undergoing or have already had pars plana vitrectomy and membrane peel combined with cataract surgery using Clareon Vivity and Clareon Vivity Toric IOLs or monofocal IOL
IOL powers between +6D to +30.0D, T3-T6
Disqualifiers
History of ocular or refractive surgery
Other ocular or systemic comorbidities that may alter or reduce visual acuity and contrast sensitivity, such as severe dry eye/ocular surface disease, glaucoma, macular degeneration, retinopathy, neuro-ophthalmic diseases, strabismus/amblyopia etc.
Patients with irregular astigmatism, corneal dystrophies, pupil abnormalities, zonular laxity
Intraoperative or postoperative complications
Trial design
Treatments tested in this trial
- cataract surgery
- retinal surgery
Treatment groups
Locations
Sponsors and collaborators
Debbie Kuo, MD
Lead sponsor
Sutter Health
Sponsor institution