Geneva, March 20 -- International Clinical Trials Registry received information related to the study (NCT07457216) titled 'Visual and Patient-Reported Outcomes After Bilateral Non-Diffractive EDOF IOL Implantation' on Feb. 27.
Study Type: Interventional
Study Design:
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: Benha University
Condition:
Extended Depth-of-Focus Intraocular Lens
Cataract
Visual Acuity
Intervention:
Device: AcrySof IQ Vivity EDOF Intraocular Lens
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: January 3, 2025
Target Sample Size: 30
Countries of Recruitment:
Egypt
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