NCT04843748

Clinical Evaluation Study for Assessing the Visual Performance of Hanita Lenses Trifocal IOL

Clinical Study for Assessing the Visual Performance of Hanita Lenses New Trifocal Intraocular Lens

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 20 (actual)
• Sponsor: Hanita Lenses · Industry
• Sex: All
• Age: 45 Years – 75 Years
• Healthy volunteers: Not accepted

Summary

Hanita Lenses Trifocal IOL, SeeLens AFR (Intensity IOL).Prospective, single-arm single-center, open-label study.

Detailed description

Device: Hanita Lenses Trifocal IOL, SeeLens AFR (Intensity IOL). Indication studied: The Hanita Lenses Trifocal IOL is intended for implantation in the capsular bag in the posterior chamber in order to replace the crystalline lens of the eye to attain visual correction of aphakia in adult patients in whom a cataractous lens has been removed, who desire improved uncorrected vision, useful near and intermediate visual functions, and reduced spectacle dependence. Study description: This study is a prospective, single-arm single-center, open-label study.

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	cataract surgery and intraocular lens implantation - both eyes	cataract surgery and intraocular lens implantation for both eyes

Timeline

• Start date: 2018-08-18
• Primary completion: 2021-01-06
• Completion: 2021-01-06
• First posted: 2021-04-14
• Last updated: 2021-04-14

Locations

1 site across 1 country: Israel