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A Comparison of the Visual Performance of Trifocal Versus Extended Depth of Focus Intraocular Lenses

A Randomized, Controlled, Two-armed, and Single Blind Trial Evaluating the Visual Performance and Quality of Vision After Bilateral Implantation of 2 Presbyopia Correcting Intraocular Lenses: Trifocal Versus Extended Depth of Focus

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03726606
Enrollment
36
Registered
2018-10-31
Start date
2018-11-05
Completion date
2019-05-06
Last updated
2018-10-31

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

Conditions

Cataract, Lenses, Visual Impairment

Keywords

Cataract, Intraocular lenses, Trifocal intraocular lenses, Extended depth of focus intraocular lenses, Presbyopia

Brief summary

We are conducting a trial evaluating the performance of trifocal versus extended depth of focus intraocular lenses. These lenses will be implanted in otherwise healthy individuals with visual problems due to bilateral cataracts. Patients must be seeking an improvement in their visual performance with a special focus on presbyopia correction.

Detailed description

To compare the clinical performance, quality of vision and subjective outcomes between the extended depth of focus (EDOF) Mini Well Ready intraocular lens (IOL) and the diffractive trifocal PanOptix IOL, at 3 months following second eye implantation. Statistical analysis All data will be analyzed using the Statistical Package for the Social Sciences (SPSS) v23 (SPSS Inc., Chicago, IL, USA). Graphs will be made using SPSS and Microsoft Excel (Microsoft Corp., Redmond, WA, USA). Normality will be tested for using the Shapiro Wilk test. If the data is normal, an independent t test will be used for comparing the continuous variables between the groups. If the data is not normal, then we will utilize the Mann Whitney U test. Sample size calculation The sample size calculation was based on the mean binocular Uncorrected Near Visual Acuity (UNVA) tested at 40cm under photopic condition. A previous study on the same diffractive trifocal IOL revealed a binocular UNVA of 0.01 ± 0.087 logMAR (12). The anticipated mean value for Mini Well Toric Ready is 0.10 logMAR. Based on these assumptions, an alpha of 0.05 and power of 0.8, it was calculated a number of 15 patients implanted bilaterally for each group. Assuming a dropout rate of 20% on the primary outcome measure, this resulted in a total number of 36 bilateral patients, 18 each group. Duration of the project: Six months to one year

Interventions

DEVICEIntraocular lens

Bilateral implantation of the same intraocular lens.

Sponsors

SIFI SpA
CollaboratorINDUSTRY
Hashmanis Foundation
CollaboratorUNKNOWN
Hashmanis Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

The patient and the examiner will be blinded to the arms.

Intervention model description

Participants will be randomly allocated to one of two arms: Trifocal or extended depth of focus intraocular lenses.

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patient aged 30 years of age or older * Has bilateral cataracts with visual problems * Is motivated for vision correction

Exclusion criteria

* Any ocular pathology that could impair vision, for example: * Pseudoexfoliation syndrome * Zonular weakness * Retinal or corneal dystrophies * Retinal pathologies like age related macular degeneration * History of trauma * History of ocular surgery * Individuals having trouble understanding written or spoken language * Those with dense cataracts causing problems with optical biometry * Average corneal powers outside the range of 41 diopters (D) to 46 D * Corneal astigmatism \> 0.75 D * Irregular astigmatism index of 0.54 or higher

Design outcomes

Primary

MeasureTime frameDescription
Near Visual Acuity (Corrected and Uncorrected)3 months after bilateral implantation40 cm
Intermediate Visual Acuity (Corrected and Uncorrected)3 months after bilateral implantation66 cm
Distance Visual Acuity (Corrected and Uncorrected)3 months after bilateral implantation4 m

Secondary

MeasureTime frameDescription
Defocus Curve3 months after bilateral implantationEvaluating presbyopia correction
Objective Automated Refraction3 months after bilateral implantationUsing a auto refractometer (Topcon KR-800, Tokyo, Japan)
Contrast Sensitivity3 months after bilateral implantationAt 2.5 m
Higher Order Abberations3 months after bilateral implantationUsing a Abberometer
Halos and Glares3 months after bilateral implantationUsing custom software provided by SIFI

Contacts

Primary ContactNauman Hashmani, MBBS
naumanhashmani@hashmanis.edu.pk00923212828062
Backup ContactSharif Hashmani, FCPS
yashhashmani@hotmail.com00923008255771

Outcome results

None listed

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