Visual Function of Enhanced Monofocal Intraocular Lenses

Sponsor
Vienna Institute for Research in Ocular Surgery
Study ID
NCT07262021
Status
Not Yet Recruiting

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Conditions

  • Cataract

Eligibility Criteria

Sex
ALL
Age
21 Years - 105 Years
Healthy Volunteers
Not accepted

Interventions

  • enhanced monofocal IOL — DEVICE
    Art 25 IOL, enhanced monofocal IOL
  • enhanced monofocal IOL — DEVICE
    Eyhance IOL, enhanced monofocal IOL

Study Details

Comparison of the visual function of two enhanced monofocal intraocular lenses after cataract surgery

Key Dates

First listed
Dec 3, 2025
Start date
Dec 1, 2025
Status verified
Nov 2025
Primary completion
Nov 1, 2026
Completion
Nov 1, 2027

Study Design

Enrollment
30 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Art 25 IOL
    Patient will receive the Art 25 IOL during cataract surgery
  • Experimental: Eyhance
    Patient will receive the Eyhance IOL during cataract surgery

Primary Outcome Measure

Distance-corrected intermediate visual acuity [ Time Frame: 3 months ]

Central Contacts

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