Outcomes of Combined Cataract Surgery With Retinal Surgery for Visually Significant Epiretinal Membrane With Vivity Versus Monofocal Intraocular Lens

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDebbie Kuo, MD

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

36 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Debbie Kuo, MD

Lead sponsor

Sutter Health

Sponsor institution