Comparison of Two Non- Diffractive Extended Depth of Focus Intraocular Lenses (NCT06607848) | Clinical Trial Compass
RecruitingNot Applicable
Comparison of Two Non- Diffractive Extended Depth of Focus Intraocular Lenses
Austria40 participantsStarted 2024-07-29
Plain-language summary
Intra-individual comparison of the PureSee EDOF IOL with the Acunex Vario EDOF IOL set for emmetropia.
Who can participate
Age range21 Years – 105 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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
* Normal findings in the medical history and physical examination unless the investigator considers an abnormality to be clinically relevant
* Written informed consent prior to surgery
Exclusion Criteria:
* 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
* Pronounced dry eye disease
* Previous ocular surgery or trauma
* Persons who are pregnant or nursing (pregnancy test will be taken in women of reproductive age)
What they're measuring
1
Distance corrected visual acuity for intermediate distance
Timeframe: 6 months
Trial details
NCT IDNCT06607848
SponsorVienna Institute for Research in Ocular Surgery