Clinical Trial on the Visual Function of Enhanced Monofocal and EDoF Intraocular Lenses
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
- Study ID
- NCT07715071
- Status
- Not Yet Recruiting
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Conditions
- Cataract
Eligibility Criteria
- Sex
- ALL
- Age
- 45 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Intraocular lens — DEVICEImplantation of intraocular lens
Study Details
Randomized clinical trial to evaluate the visual performance of enhanced monofocal and extended depth-of-field intraocular lenses
Key Dates
- First listed
- Jul 20, 2026
- Start date
- Sep 21, 2026
- Status verified
- Jul 2026
- Primary completion
- Mar 31, 2027
- Completion
- Mar 31, 2027
Study Design
- Enrollment
- 90 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Group 1: Implantation of the Clareon Vivity intraocular lensEDoF IOL
- Experimental: Group 2: Implantation of the TECNIS Eyhance intraocular lensEnhanced monofocal IOL
- Experimental: Group 3: Implantation of the RayOne EMV intraocular lensEnhanced monofocal IOL
- Experimental: Group 4: Implantation of the IsoPure Serenity intraocular lensEnhanced monofocal IOL
- Experimental: Group 5: Implantation of the Vivinex Impress intraocular lensEnhanced monofocal IOL
- Experimental: Group 6: Implantation of the TECNIS PureSee intraocular lensEDoF IOL
Primary Outcome Measure
Visual acuity at different distances [ Time Frame: 1 month, 3 months, 6 months ]
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