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Clinical Trials/NCT04800887
NCT04800887
Completed
Not Applicable

Comparison of Visual Outcomes and Contrast Sensitivity in Patients Implanted With Tecnis Eyhance IOL (Intraocular) and Tecnis Monofocal IOL

Faculty Hospital Kralovske Vinohrady1 site in 1 country22 target enrollmentNovember 12, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intraocular Lens
Sponsor
Faculty Hospital Kralovske Vinohrady
Enrollment
22
Locations
1
Primary Endpoint
Comparison of visual acuity between eyes implanted with EDOF IOL and eyes implanted with monofocal IOL
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

To compare visual outcomes for various distances, reading speed, contrast sensitivity, glare occurence, defocus curve and subjective satisfaction in patients implanted with the extended depth of focus lens (Tecnis Eyhance) in one eye and monocal aspheric lens (Tecnis ZCB00) in second eye. Patients undergo visit in 3,6 and 12 months after the surgery.

Detailed Description

The goal of refractive cataract surgery is to remove the opacity, or cataract and to produce the desired refractive outcome. In most cases, the desired outcome is an emmetropic eye, or an eye that sees 20/20 Snellen for distance vision post-surgery with the implant of a monofocal IOL. This, however, does not offer much in the way of intermediate and near vision. The increased desire for simultaneous distance, intermediate and near vision has increased the popularity of multifocal IOLs (MIOLs). However MIOLs provide visual acuity for all distances, they has occurence of optical phenomena such as glare and halo and lower contrast sensitivity. Extended depth of focus (EDOF) lens should provide distance vision as good as monofocal lens and intermediate vision better than monofocal but without any optical phenomenon or decreased contrast sensitivity. This study is conducted from 11/2019 to 08/2021 in the Ophthalmology department of Faculty Hospital Kralovske Vinohrady in Prague. The research protocol was explained to all participants and informed consent was signed before enrolling patient to the study. The study was approved by the Ethics Committee of Faculty Hospital Kralovske Vinohrady and will enrolled up to 25 patients with presence of cataract in both eyes. Bilateral clear corneal phacoemulsification and IOL implantation is performed by one surgeon using the same technique in both eyes. The surgical process involved topical anesthesia, superior 3-step clear corneal incision (2,2mm), 5,0mm curvilinear capsulorhexis, phacoemulsification, bilateral irrigation- aspiration and IOL implantation. One eye is implanted with EDOF IOL second eye with monofocal IOL. Type of IOL is chosen randomly and double masked. Patients are scheduled for visit at 3,6 and 12 months after the surgery.

Registry
clinicaltrials.gov
Start Date
November 12, 2019
End Date
August 24, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Faculty Hospital Kralovske Vinohrady
Responsible Party
Principal Investigator
Principal Investigator

Andrea Janekova

MD

Faculty Hospital Kralovske Vinohrady

Eligibility Criteria

Inclusion Criteria

  • presence of cataract in both eyes
  • no other ocular pathology affecting visual acuity
  • bilateral phacoemulsification cataract surgery was arranged for both eyes
  • corneal astigmatism up to 0,75 cylinder (measured by IOL Master biometry)
  • dioptric power of both selective lens within 1,5 D range in one patient
  • selecting IOL power between 18 D and 27 D power range

Exclusion Criteria

  • complicated cataract
  • corneal opacities or irregularities
  • amblyopia
  • anisometropia
  • coexisting ocular pathologies
  • history of ocular surgery
  • refusal or unable to maintain follow-up

Outcomes

Primary Outcomes

Comparison of visual acuity between eyes implanted with EDOF IOL and eyes implanted with monofocal IOL

Time Frame: 12 months

* uncorrected distance visual acuity (UDVA) * corrected distance visual acuity (CDVA) * uncorrected near visual acuity (UNVA) * distance corrected near visual acuity (DCNVA) * corrected near visual acuity (CNVA) * uncorrected intermediate visual acuity (UIVA) * distance corrected intermediate visual acuity (DCIVA)

Comparison of defocus curve between eyes implanted with EDOF IOL and eyes implanted with monofocal IOL

Time Frame: 6 months

A defocus curve that measures visual acuity should be obtained by using the best corrected distance refraction and then defocusing the image in 0.5 increments from +1.5 to -2.5 diopter with spherical plus and spherical minus trial lenses (i.e.,+1.5 D, +1.0 D, +0.5 D, 0.00 D, -0.5 D, -1.00 D, . . . ,-2.50 D) with visual acuity recorded at each change in correction.

Comparison of reading speed between eyes implanted with EDOF IOL and eyes implanted with monofocal IOL

Time Frame: 12 months

Monocular reading speed (Salzburg reading desk for 66cm and 80cm)

Difference in contrast sensitivity between eyes with EDOF IOL and monofocal IOL

Time Frame: 12 months

Contrast sensitivity - CSV (contrast sensitivity vision) 1000 device- monocularly, mesopic, without glare Contrast sensitivity measurement on Glaretester- monocularly- with and without glare

Secondary Outcomes

  • Change in reading speed in eyes implanted with EDOF IOL(3 and 12 months)
  • Change in contrast sensitivity in eyes implanted with EDOF IOL(3 and 12 months)
  • Questionaire(6 months)
  • Change in intermediate visual acuity in eyes implanted with EDOF IOL(3 and 12 months)

Study Sites (1)

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