Patient Preference and Visual Quality With Contralateral Synergy Versus Panoptix

The goal of this study is to compare the visual quality and patient preference of the Synergy IOL versus the PanOptix IOL when one of each lens is placed in the same patient.

Completed

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Key information

Conditions

IOL Behavior Cataract Eye Diseases Health Behavior Lens Diseases Patient Satisfaction Treatment Adherence and Compliance

Age range

40 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bucci Laser Vision Institute

Wilkes-Barre, Pennsylvania, 18702, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Bilateral cataracts for which phacoemulsification extraction and posterior IOL implantation have been planned for both eyes
Desire to mitigate postoperative presbyopia with implantation of Synergy IOL in one eye and PanOptix Trifocal IOL in the opposite eye

Exclusion criteria

Any vision-limiting problems (e.g., corneal, retinal, infection) which can potentially limit post-operative visual performance
Any ocular condition or trauma that is not resolved, stable, or would compromise the well-being of the subject

Treatment and study plan

Tecnis Synergy IOL

Device

Implanted in one eye

AcrySof PanOptix Trifocal IOL

Device

Implanted in one eye

Primary outcomes

Patient Satisfaction - subjective questionnaire

Time frame: 3 months to 18 months after cataract surgery

Subjective questionnaire explores the frequency and need for glasses for various visual functions at distance, intermediate, and near and overall satisfaction of visual function without glasses
Visual Acuity at Distance

Time frame: 3 months to 18 months after cataract surgery

Uncorrected and best corrected visual acuities measured at distance
Visual Acuity at Intermediate

Time frame: 3 months to 18 months after cataract surgery

Uncorrected and best corrected visual acuities measured at intermediate
Visual Acuity at Near

Time frame: 3 months to 18 months after cataract surgery

Uncorrected and best corrected visual acuities measured at near

Sponsors and collaborators

Lead sponsor

Bucci Laser Vision Institute

Other

Registry information

Important dates

Study start: 2022
Primary completion: 2023
Study completion: 2023
First posted: Nov 9, 2022
Registry last updated: Jul 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed