Posters

Long term clinical evaluation of visual, refractive and adverse events: outcomes of a new monofocal IOL

Poster Details

First Author: M.Teus SPAIN

Co Author(s):                     

Abstract Details

Purpose:

A prospective, multicenter, single group safety and performance clinical trial to demonstrate the long-term (3 years) visual acuity, refractive and adverse event outcomes for the Clareon IOL (Alcon). This paper presents 1-Year interim results from subjects evaluated in a single site in Spain.

Setting:

Hospital Universitario Principe de Asturias, Madrid, Spain.

Methods:

Subjects scheduled for bilateral cataract surgery with no ocular pathology other than cataract that could compromise visual function or the measurements are included. In each subject, the Clareon IOL (Model SY60WF) was implanted in both eyes. Study examinations are performed preoperatively, 1 day, 1 week, 1 month, 6 months, 1, 2 and 3 years after cataract surgeries. Best corrected distance visual acuity (BCDVA), uncorrected distance visual acuity (UCDVA), manifest refraction, Slit lamp examination, ACD, PCO assessment and IOL observations are carried out at each visit.

Results:

17 eyes of 34 patients enrolled at this site will be included. One-year study visits evaluations are still ongoing and therefore results are not available yet. Results will be shown at the Winter ESCRS meeting.

Conclusions:

We will report the visual, refractive and IOL observations of the Clareon IOL in this cohort of study subjects.

Financial Disclosure:

None