Visual Outcomes Following Bilateral Implantation of the Vivity Toric Intraocular Lens

N/ACompletedNCT06196593

LEC Eye Centre30 enrolled

Overview

The objective of this study was to evaluate the clinical and patient reported outcomes after bilateral implantation of the AcrySof™ IQ Vivity™ Toric intraocular lens.

This is a prospective interventional case series of 30 patients who underwent cataract surgery and bilateral implantation of the AcrySof™ IQ Vivity™ Toric intraocular lens. This study is represented by an Asian cohort of patients and the study evaluations were focused not only on clinical visual outcomes but also on "real-life" patient reported outcomes such as dysphotopsias, spectacle independence and daily visual tasks all of which were measured at 1 month and up to 3 months postoperatively. The objective would be to provide insight into the performance of this intraocular lens in Asian patients.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Cataract Senile Intraocular Lens Complication

Interventions

AcrySof™ IQ Vivity™ Toric intraocular lensDEVICE

Uneventful phacoemulsification and implantation of IOL

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * patients aged 18 years or older * bilateral significant cataracts * bilateral significant corneal astigmatism Exclusion Criteria: * previous refractive surgery * amblyopia * strabismus * any ocular co-morbidity which could impact on final visual acuity * pre-existing zonular weakness * capsular instability or compromise

Locations (1)

LEC Eye Centre

Ipoh, Perak, Malaysia

Outcomes

Primary Outcomes

Binocular UDVA

Binocular Uncorrected Distance Visual Acuity

Time frame: 3 months

Binocular UIVA

Binocular Uncorrected Intermediate Visual Acuity

Time frame: 3 months

Binocular UNVA

Binocular Uncorrected Near Visual Acuity

Time frame: 3 months

Secondary Outcomes

CDVA

Corrected Distance Visual Acuity

Time frame: 3 months

DCIVA

Distance Corrected Intermediate Visual Acuity

Time frame: 3 months

DCNVA

Distance Corrected Near Visual Acuity

Time frame: 3 months

MRSE

Mean Refractive Spherical Equivalent

Time frame: 3 months

Rotational Stability

Degree of rotation of intraocular lens

Time frame: 1 month

Binocular Defocus Curve

Measurement of the performance of the Intraocular lens at different distances

Time frame: 3 months

Contrast Sensitivity

Measurement of the contrast sensitivity after implantation with this intraocular lens

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.