NCT05573529

EDOF and Multifocal IOL Study

Comparison of Visual Outcomes and Patient Satisfaction After Bilateral Implantation of EDOF and Multifcoal IOLs- a Prospective Randomized Controlled Trial

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 50 (actual)
• Sponsor: Medical University of Vienna · Academic / Other
• Sex: All
• Age: 50 Years – 90 Years
• Healthy volunteers: Not accepted

Summary

The investigational devices are approved intraocular lenses (IOLs) intended to be implanted after phacoemulsification in individuals suffering from age-related cataract with the need of cataract surgery. Cataract surgery with precedent bilateral randomized IOL implantation will be performed in subjects who have signed an informed consent form. Postoperative examinations will be implemented in accordance with the approved investigational plan.

Conditions

• Age-related Cataract

Interventions

Type	Name	Description
PROCEDURE	phacoemulsification and intraocular lens implantation	bilateral cataract surgery including phacoemulsification in individuals suffering from age-related cataract and intraocular lens implantation
DEVICE	intraocular lens implantation	intraocular lens implantation includes EDOF IOL implantation in the dominant eye and multifocal IOL implantation in the non-dominant eye after phacoemulsification

Timeline

• Start date: 2020-11-09
• Primary completion: 2023-03-23
• Completion: 2025-02-05
• First posted: 2022-10-10
• Last updated: 2025-06-18

Locations

1 site across 1 country: Austria