Mix and Match Study of Two Multifocal Intraocular Lens With Different Add Power

tae-young chung40 enrolled

Overview

To assess postsurgical visual acuity (distant, intermediate, near), refractive errors, contrast sensitivity, visual function and patient satisfaction after implantation of multifocal IOLs of different add power contralaterally.

Multifocal intraocular lens (MIOL) is considered a prevailing alternative to restore the functional vision from far to near independent of glasses. Many clinical studies on diffractive MIOLs, refractive MIOLs, or hybrid MIOLs in enhancing quality of vision showed promising outcomes. Several studies have confirmed the satisfactory visual outcomes of Tecnis MIOL with +4.00 D add power. The purpose of study is to assess the visual performance after cataract surgery with bilateral implantation of multifocal IOL with two different add power (+2.75 D or +3.25 D) in one patient.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Presbyopia

Interventions

Phacoemulsification with multifocal intraocular lensDEVICE

Phacoemulsification and implantation of a multifocal intraocular lens (IOL) with two different add power (+2.75 diopters (D) or +3.25 D, respectively) in each eye of a patient, contralaterally. They're called mix and matched patients.

Eligibility

Sex: ALLMin age: 20 YearsMax age: 70 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * • Age-related cataract * Adult at the age of 21 or older at the time of the pre-operative examination and willing to have surgery on their 2nd eye within 7-28 days of their 1st eye. * A patient has the visual potential of 20/25 or better in each eye after cataract removal and IOL implantation. * A patient with preoperative corneal astigmatism from IOL Master less than 1 diopters * Written informed consent to surgery and participation in the study Exclusion Criteria: * • Pregnant woman and lactating woman * A patient with history of retinal disease * A patient with history of ocular trauma or ocular surgery (Intraocular surgery, refractive surgery, ocular surface surgery) in either eye * A patient with evidence of keratoconus or significant irregular astigmatism on pre-operative topography in either eye. * A patient that has been wearing PMMA lenses within 6 months, gas permeable lenses within one month, or extended -wear or daily soft contact lens within 7 days of their scheduled surgery. * Those with other diseases that can affect capsule stability such as pseudoexoliation syndrome, glaucoma, traumatic cataract, or marfan syndrome * Those who are not able to read and understand the informed consent (illiterate or foreigners)

Outcomes

Primary Outcomes

Visual acuity(Distant, intermediate, near)

Time frame: 1month

Secondary Outcomes

Visual acuity(Distant, intermediate, near)

Time frame: 3month

Data from ClinicalTrials.gov

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