Vivity Outcomes in Patients With Early Stage Glaucoma

Vance Thompson Vision27 enrolled

Overview

The goal of the study is to determine the visual outcomes in patients with mild, pre-perimetric glaucoma who undergo cataract surgery with implantation of the Alcon Vivity Extended Range Intraocular Lens (IOL).

Study Type

OBSERVATIONAL

Enrollment

Conditions

Glaucoma Cataract Presbyopia

Interventions

Cataract Surgery with Implantation of Vivity Extended Range of Vision IOLPROCEDURE

Patients with early stage glaucoma implanted with Vivity or Vivity Toric IOL

Eligibility

Sex: ALLMin age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients at least age 45 years of age undergoing uncomplicated cataract surgery with optional concomitant minimally invasive glaucoma surgery (MIGS) 2. Subjects with documented diagnosis of pre-perimetric glaucoma 3. Calculated lens power within Vivity/Vivity toric range 4. Willing and able to comprehend informed consent and complete 4-6 month post-op visit 5. Potential postoperative BCDVA of 20/20 or better in each eye based on Investigator's medical opinion Exclusion Criteria: 1. Ocular comorbidity, other than pre-perimetric glaucoma, that could reduce the potential postoperative BCDVA 2. Previous ocular surgery including refractive surgery 3. Subjects who are pregnant or plan to become pregnant during the course of the study.

Locations (1)

Vance Thompson Vision

Sioux Falls, South Dakota, United States

Outcomes

Primary Outcomes

Uncorrected Distance Visual Acuity

Time frame: 4-6 months

Uncorrected Intermediate Visual Acuity

Time frame: 4-6 months

Uncorrected Near Visual Acuity

Time frame: 4-6 months

Secondary Outcomes

Contrast Sensitivity

As measured by Pelli Robson Chart

Time frame: 4-6 months

Patient Satisfaction and Spectacle Independence Survey Results

Time frame: 4-6 months

Mean Refractive Spherical Equivalent

Time frame: 4-6 months

Data from ClinicalTrials.gov

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