RecruitingNot ApplicableNCT06345820
Comparison of Two Non-diffractive Enhanced Monofocal Intraocular Lenses
Intermediate Visual Acuity Comparison of Two Non-diffractive Enhanced Monofocal Intraocular Lenses
Sponsor
Vienna Institute for Research in Ocular Surgery
Enrollment
35 participants
Start Date
Jun 28, 2023
Study Type
INTERVENTIONAL
Conditions
Summary
Comparison of the clinical performance of two enhanced monofocal IOLs with similar design.
Eligibility
Min Age: 21 YearsMax Age: 105 Years
Inclusion Criteria7
- Bilateral cataract
- Age 21 or older
- Visual acuity > 0.05
- Axial length: 22.00-26.00mm
- Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically irrelevant
- Written informed consent prior to surgery
- Availability, willingness and sufficient cognitive awareness to comply with examination procedures
Exclusion Criteria7
- Active ocular disease (e.g. chronic uveitis, proliferative diabetic retinopathy, chronic glaucoma not responsive to medication)
- Relevant other ophthalmic diseases such as pseudoexfoliation syndrome (PEX), Intraoperative Floppy Iris Syndrome (IFIS)
- Corneal decompensation or corneal endothelial cell insufficiency
- Amblyopia
- Previous ocular surgery or trauma
- Persons who are pregnant or nursing (pregnancy test will be taken in women of reproductive age)
- Astigmatism with the need for a toric IOL
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Interventions
DEVICEEvolux
Evolux, enhanced monofocal IOL
DEVICETecnis Eyhance
Tecnis Eyhance, enhanced monofocal IOL
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06345820
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