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Clinical Outcomes Following Implantation of Tecnis Synergy and Symfony Intraocular Lens

CompletedNA

Sponsor: George O. Waring IV

Conditions: Cataract

Interventions: Intraocular lens

Countries: United States

Tecnis Symfony Optiblue (Johnson \& Johnson Vision, Santa Ana, CA, Unites States) is a violet light filtering extended depth of focus intraocular lens (IOL) that provides a continuous range of clear vision at far and intermediate. Tecnis Synergy™ IOL (Johnson \& Johnson Vision, Santa Ana, CA, Unites States) is another latest United States Food and Drug Administration (USFDA) approved IOL, designed to provide good acuity at far through near distances, reducing the need for spectacles. These IOLs are approved/licensed for use and are not investigational. The present study intends to evaluate the clinical outcomes and patient satisfaction following contralateral implantation of Tecnis Synergy and Symfony Optiblue in cataract patients. The investigator hypothesizes that the contralateral implantation of these two lenses will allow a good proportion of patients to be spectacle independent at distance, intermediate, and near. The findings of this study may help the surgeons make better decisions on the choice of IOL in the future.

Eligibility overview

Sex: ALL

Age: 40 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Inclusion Criteria:

* Age 40 years or older
* Requiring bilateral cataract surgery, wish to achieve spectacle independence.
* Are suitable candidates for Tecnis Synergy and Tecnis Symfony IOLs
* Have predicted postoperative astigmatism ≤ 0.75 D
* Willing to provide written informed consent and adhere to study requirements

Exclusion Criteria:

* History of ocular surgery, including laser refractive surgery
* History of ocular trauma
* Patients planning for any concomitant ocular procedure at the time of cataract surgery (including MIGS) other than incisional correction of astigmatism as the time of surgery
* Ocular comorbidities including glaucoma, macular degeneration, corneal scars, or any other condition that might limit the ability to achieve 20/20 visual acuity.
* Unwillingness to provide written informed consent,
* Disability to understand and/or fill the patient questionnaire,
* Pregnancy or lactation.
* Any patient who meets enrollment criteria but subsequently experiences an intraoperative complication or does not undergo surgery with implantation of the intended pair of IOLs will also be excluded.

Locations (1)

Mt. Pleasant, South Carolina, United States