Assessment of Visual Performance Combining a Symfony IOL and a +3.25 Tecnis Multifocal IOL

Crystal Clear Vision

Status: Completed

Conditions: Cataract

Treatments: Procedure: Cataract Surgery

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02847572

CrystalClearVision

Details and patient eligibility

About

This will be a single center, non comparison clinical trial. Fifty study patients will have the Symfony IOL implanted in their dominant eye and a +3,25D Tecnis Multifocal in their non-dominant eye. The investigators will be evaluated vision at distance, intermediate and near as well as assessing patient satisfaction and spectacle independence.

Full description

Each study patient will undergo the same routine cataract extraction procedure in each eye. In their dominant eye a Tecnis Symfony IOL will be implanted and in the non dominant eye, a Tecnis +3.25D Multifocal implanted. The surgeries will be within 2 days of each other. Every patient will receive same postoperative instructions and medications. The aim is to investigate the potential benefits of implanting two different IOL's to give the patient a wider range of near vision with decreased risk of haloing and glare to enable them to be less dependent on reading glasses

Enrollment: 50 patients

Sex: All

Ages: 21+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• good general health,
• willing to comply with study instructions,
• Visual potential of 20/30 or better,
• less than 1.5D of corneal astigmatism,
• normal macula,
• clear lens or cataract,
• pupil size greater than 3.5mm

Exclusion criteria

• known pathology to affect visual outcome,
• amblyopia or strabismus,
• pupil abnormalities,
• zonule problems,
• keratoconus,
• no prior ocular surgery,use of medication that could affect vision,
• uncontrolled systemic disease

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Surgery Patient

Other group

Description:

All patients to be implanted bilaterally with a Tecnis Extended Range Lens in the Dominant eye and a Low Add Multifocal in the non dominant

Treatment:

Procedure: Cataract Surgery