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Vivity Insight: A Study of Patient Satisfaction and Visual Performance

Vivity Insight: A Study of Patient Satisfaction and Visual Performance

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04495049
Enrollment
60
Registered
2020-07-31
Start date
2020-08-01
Completion date
2021-04-30
Last updated
2021-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract

Brief summary

This will be a single arm, open-label, prospective study of patient-reported outcomes of patients with bilateral implantation of the Vivity or Vivity Toric implant.

Detailed description

Existing diffractive extended depth of focus (EDOF) lenses provide two adjacent zones of uncorrected vision (distance and intermediate or intermediate and near) but have a track record of frequent patient dissatisfaction because of unwanted visual side effects, spider webs or haloes. The Vivity non-diffractive EDOF lens offers this same range ofvision with contrast sensitivity similar to a monofocal lens, which suggests fewer side effects will be encountered in clinical practice. This study is designed to measure postoperative patient-reported outcomes with this new lens implant. Previous studies we have conducted on the bilateral ReSTOR 3.0, ReSTOR with ActiveFocus 2.5 (mixed with 3.0 and alone with mini-monovision) have shown high satisfaction, spectacle independence, and acceptable glare and halo profiles using a validated questionnaire instrument developed by MDbackline, Inc. The postoperative portions of this study will be designed to mirror those previous studies using the same instrument. All subjects will receive the Vivity or Vivity Toric implant binocularly with a target of plano sphere.

Interventions

DEVICEAlcon Vivity or Vivity Toric IOL

Patients who previously underwent cataract surgery with the Alcon Vivity or Vivity Toric IOL in both eyes.

Sponsors

Research Insight LLC
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients with cataract and otherwise healthy eyes, not exhibiting any significant ocular morbidity that would be expected to influence outcome measures. * Patients implanted with Vivity or Vivity Toric lenses bilaterally within 6 months of the survey administration. * Patients whose postoperative manifest refraction at the time of the survey is within ± 0.5 D sphere and ≤0.75 D of cylindrical refraction. * Patients who have given consent to participate in the survey.

Exclusion criteria

* Patients with visually significant co-morbidities (corneal, retina, optic nerve disease) that could affect their satisfaction with surgery. * Patients with surgical complications either during or after surgery (capsule tears, iris trauma, decentered IOL, cystoid macular edema, etc.) that would, the judgement of the investigator, influence the outcome measures of the study. * Patients with previous refractive surgery within the past 6 months prior to cataract surgery. * Patients with \> grade 1 posterior capsule opacity at their last visit. * Patients who do not meet the refractive endpoints described in the Inclusion Criteria.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients reporting not at all or just a little when asked, With or without glasses, how much do you notice glare or haloes around lights in dim light situations?8/1/2020 - 7/1/2021Percentage of patients reporting not at all or just a little when asked, With or without glasses, how much do you notice glare or haloes around lights in dim light situations?

Secondary

MeasureTime frameDescription
Percentage of postoperative patients who report rarely when asked How often do you need glasses to see the computer?8/1/2020 - 7/1/2021Percentage of postoperative patients who report rarely when asked How often do you need glasses to see the computer?
Percentage of postoperative patients who report that they do not require reading glasses for various activities8/1/2020 - 7/1/2021Percentage of postoperative patients who report that they do not require reading glasses for various activities (driving, reading, including fine print, seeing computer monitor, watching TV, sports/hobbies when asked For what types of activities do you need glasses to see (other than sunglasses)?

Other

MeasureTime frameDescription
Percentage of patients reporting very satisfied when asked, Overall, how satisfied are you with your vision after your latest surgery?8/1/2020 - 7/1/2021Percentage of patients reporting very satisfied when asked, Overall, how satisfied are you with your vision after your latest surgery?
Percentage of patients who report very satisfied or satisfied to the same question.8/1/2020 - 7/1/2021Percentage of patients who report very satisfied or satisfied to the same question.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026