Comparison of Two Non- Diffractive Extended Depth of Focus Intraocular Lenses

ConditionCataract

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age21-105

SponsorVienna Institute for Research in Ocular Surgery

About this trial

Intra-individual comparison of the PureSee EDOF IOL with the Acunex Vario EDOF IOL set for emmetropia.

Eligibility criteria

Qualifiers

Age-related bilateral cataract

Age 21 or older

Visual acuity > 0.05

For patients with regular corneal astigmatism greater than or equal to 1.00 dpt toric IOLs will be implanted

Disqualifiers

Active ocular disease (e.g chronic uveitis, diabetic retinopathy, chronic glaucoma not responsive to medication, corneal dystrophies, etc.) precluding good post-operative visual acuity

Relevant other ophthalmic diseases such as pseudoexfoliation syndrome (PEX)

Corneal decompensation or corneal endothelial cell insufficiency

Irregular astigmatism on corneal tomography

Trial design

Treatments tested in this trial

Low-Add EDOF IOL
EDOF IOL

Treatment groups

40 Participants

are divided into 2 treatment groups

Sponsors and collaborators

Vienna Institute for Research in Ocular Surgery

Lead sponsor

Source ClinicalTrials.gov