Reading Performance in Patients With Acrysof IQ Vivity Versus Acrysof IQ

NCT ID: NCT05194657

Last Updated: 2022-01-18

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 68 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-03
• Study Completion Date: 2024-01-03

Brief Summary

Comparison of the visual function and reading performance between the Acrysof IQ Vivity IOL, an EDOF IOL, and the monofocal Acrysof IQ.

Detailed Description

With increasing demands of patients concerning their visual function after cataract surgery, a variety of advanced technology intraocular lenses (IOL) have become available in the last years. Various developments aim at a reduced spectacle independence for patients after cataract or refractive lens surgery.

Novel technology for providing an extended depth of focus (EDOF) has been developed to account for unmet needs of patients. A novel EDOF IOL, the Acrysof IQ Vivity, has two surface transition elements that work simultaneously by stretching and shifting the wavefront to create a continuous extended focal range instead of multiple focal points.

To assess the performance of such an IOL technology, most studies assess visual acuity at different distances from far, to intermediate up to near. Since most activites with digital devices implicate reading, it is not surprising that reading difficulty is the most common complaint among individuals experiencing visual disturbances with multifocal designs.

Reading ability is usually evaluated using various reading tests that assess reading speed and reading acuity defined as the print size that can stell be read with sufficient speed. However, one of the fundamental problems of these tests is that reading speed is also influenced by the average amount of time that a patient reads as well as the language of the text, whether it is the first or second language.

A novel method to analyse reading performance that appears to be more objective and less reliant on the cognitive abilities of the patient is the observation of the reading pattern using a high-speed eye-tracking system that analyses eye fixations during the reading test. In previous studies we have seen that several aspects of this reading patter, i.e. fixation duration and fixation frequency, appear to correlate with the reading performance overall and can be differentially used to discriminate between cognitive and visuo-motor processing.

Hence, the aim of this study is to assess the visual function and reading performance with an EDOF IOL (Acrysof IQ Vivity) compared to a standard monofocal IOL (Acrysof IQ).

136 eyes of 68 patients will be included into this study. According to the randomization, 34 patients will be implanted with the Acrysof IQ Vivity in both eyes and the other 34 patients will be implanted with the Acrysof IQ in both eyes. A follow-up examination will be performed at 3 months postoperative. During this visit a slitlamp examination, biometry and tomography of the eye, refraction and visual acuity assessment, an OCT examination, a retroillumination photogrypha, reading speed analysis and halometry will be performed.

Conditions

Cataract

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Acrysof IQ Vivity

Patient will receive the enhanced depth of focus IOL during cataract surgery

Group Type: EXPERIMENTAL

enhanced depth of focus IOL

Intervention Type: DEVICE

Acrysof IQ Vivity, enhanced depth of focus IOL

Acrysof IQ

Patiet will receive the monofocal IOL during cataract surgery

Group Type: EXPERIMENTAL

monofocal IOL

Intervention Type: DEVICE

Acrysof IQ, monofocal IOL

Interventions

enhanced depth of focus IOL

Acrysof IQ Vivity, enhanced depth of focus IOL

Intervention Type: DEVICE

monofocal IOL

Acrysof IQ, monofocal IOL

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Cataract
• Stereopsis
• age 21 and older
• regular corneal astigmatism of up to 3.0 D
• written informed consent prior to surgery
• normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
• availability, willingness and sufficient cognitive awareness to comply with examination procedures
• german as mother-tongue
• calculated IOL power needed is below 15.0 D or above 25.0 D (no high myopia or high hypermetropia will be recruited)

Exclusion Criteria

• relevant other ophthalmic diseases such as: pseudoexfoliation, glaucoma, traumatic cataract, corneal scars, and other co-morbidity that could affect capsule bag stability (e.g. Marfan syndrome) or retinal diseases affecting visual acuity (AMD, Macular Pucker, post-operative macular edema...)
• amblyopia
• contact lenses
• irregular corneal astigmatism on corneal topography
• postoperative subjective refraction smaller/ higher than or 0.75 D
• pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 105 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Vienna Institute for Research in Ocular Surgery

OTHER

Sponsor Role: lead

Responsible Party

Prim. Prof. Dr. Oliver Findl, MBA

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Oliver Findl, MD

Role: PRINCIPAL_INVESTIGATOR

Vienna Institute for Research in Ocular Surgery (VIROS), Hanusch Hospital Vienna

Locations

Vienna Institute for Research in Ocular Surgery (VIROS), Hanusch Hospital Vienna

Vienna, , Austria

Site Status: RECRUITING

Countries

Austria

Central Contacts

Sahand Amir-Asgari, MD

Role: CONTACT

office@viros.at

01 91021 ext. 57564

Natascha Bayer, MSc

Role: CONTACT

office@viros.at

01 91021 ext. 57564

Facility Contacts

Sahand Amir-Asgari, MD

Role: primary

office@viros.at

01 91021 ext. 57564

Natascha Bayer, MSc

Role: backup

office@viros.at

01 91021 ext. 57564

Other Identifiers

Vivity

Identifier Type: -

Identifier Source: org_study_id