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Comparison of Premium Monovision and Bilateral Implantation of Trifocal Diffractive Intraocular Lenses

Comparative Study of Premium Monovision and Bilateral Implantation of Trifocal Diffractive Intraocular Lenses

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05494177
Enrollment
100
Registered
2022-08-09
Start date
2022-08-01
Completion date
2023-03-01
Last updated
2023-06-18

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

Conditions

Presbyopia, Refractive Errors, Cataract

Keywords

pseudophakic presbyopic correction, premium monovision, trifocal diffractive intraocular lenses, extended depth of field intraocular lenses

Brief summary

Primary objective of this study is to compare two presbyopia correction surgical techniques, specificaly premium monovision, in which the dominant eye is corrected with an extended depth of field intraocular lens and the non-dominant eye with a trifocal diffractive intraocular lens, and the bilateral implantation of trifocal diffractive intraocular lenses.

Detailed description

Two study groups will be formed. The first group will include patients who undergone premium monovision and the second will include patients who undergone bilateral implantation of trifocal diffractive intraocular lenses. Patients who have undergone one of the aforementioned categories of presbyopia correction surgery will be selected in order to compare the effectiveness of these techniques by evaluating uncorrected near, intermediate and distant visual acuity, uncorrected Critical Print Size (CPS) in near and intermediate distance, dysphotopic phenomena (glare, halos) through a 4-level severity scale by patients, contrast sensitivity, the need of use glasses for all distances or separately for activities requiring near or distant vision as well as the degree of subjective satisfaction of patient via interview (NEI-VFQ 25). The purpose of measuring these parameters is to calculate, through a mathematical model, the relative effectiveness of each method.

Interventions

DIAGNOSTIC_TESTbUDVA, bUIRA, bUNRA, bUICPS, bUNCPS

All participants will be assessed on the following clinical indexes: 1. Binocular uncorrected distant visual acuity (bUDVA) at four meters distance 2. Binocular uncorrected intermediate reading acuity (bUIRA) at 60 cm 3. Binocular uncorrected near reading acuity (bUNVA) at 40 cm 4. Binocular uncorrected intermediate Critical Print Size (bUICPS) at 60 cm 5. Binocular uncorrected near Critical Print Size (bUNCPS) at 40 cm All the above parameters are obtained using the Democritus Digital Acuity & Reading Test (DDART).

DIAGNOSTIC_TESTContrast sensitivity

Contrast sensitivity is assessed with the Pelli-Robson test.

Sponsors

Democritus University of Thrace
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of cataract with stage 2 according to the Lens Opacities Classification System III (LOCS-3) grading scale * Age\>45 years

Exclusion criteria

* Disability to understand the Greek language and respond to the interview * Fundus or corneal diseases * Glaucoma * Previous intraocular surgery

Design outcomes

Primary

MeasureTime frameDescription
Binocular uncorrected near critical print size (bUNCPS)1 yearbUNCPS is obtained using the near vision test of DDART at 40 cm distance.
Binocular uncorrected distant visual acuity (bUDVA)1 yearbUDVA is obtained using the distance vision test of DDART at four meters distance.
Binocular uncorrected intermediate reading acuity (bUIRA)1 yearbUIRA is obtained using the near vision test of DDART at 60 cm distance.
Binocular uncorrected near reading acuity (bUNRA)1 yearbUNRA is obtained using the near vision test of DDART at 40 cm distance.
Binocular uncorrected intermediate critical print size (bUICPS)1 yearbUICPS is obtained using the near vision test of DDART at 60 cm distance.

Secondary

MeasureTime frameDescription
Contrast sensitivity1 yearContrast sensitivity is evaluated with the Pelli-Robson test.
Spectacle independence1 yearSpectacle dependence is assessed for both distant and near vision by two direct 4-scale Likert-type questions (Always, Most of the times, Sometimes, Never).
Subjective satisfaction using Visual Function Index (VF-14) (total score, VF14-Near Vision (NV) score & VF14-Distance Vision (DV) score)1 yearSubjective satisfaction rates are assessed using the prevalent VF-14 questionnaire. Further to the total VF-14 score assessment, two additional scores are calculated: a) Near vision VF score (VF14-NV) derived from items that assess the perceived difficulty in near vision activities (items 1,2,3,7,8,9 and 11), and, b) Distant vision VF score (VF14-DV) derived from items that assess the perceived difficulty of distant vision activities (items 4, 5, 6, 10, 12, 13 and 14). VF-14 has a final score from 0 to 100. A score of 100 indicates able to do all applicable activities. A score of 0 indicates unable to do all applicable activities because of vision.
Dysphotopsia symptoms1 yearDysphotopsia is evaluated with two direct 4-scale, Likert-type questions (Always, Most of the times, Sometimes, Never) assessing subjective appearance of glare and halos.

Countries

Greece

Outcome results

None listed

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