NCT02691741

Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal Intraocular Lenses (IOL)

Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal IOLs

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 215 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 22 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to clinically evaluate the visual performance of two commercially available presbyopia-correcting Trifocal IOLs.

Detailed description

Subjects will attend a total of 9 visits (6 postoperative) over a 7 month period.

Conditions

• Cataracts

Interventions

Type	Name	Description
DEVICE	AcrySof® IQ PanOptix™ Presbyopia-Correcting IOL	Trifocal IOL(near, intermediate, distance) implanted for long-term use over the lifetime of the cataract patient
DEVICE	AT LISA® tri IOL	Trifocal IOL(near, intermediate, distance) implanted for long-term use over the lifetime of the cataract patient

Timeline

• Start date: 2016-04-29
• Primary completion: 2017-07-17
• Completion: 2017-07-17
• First posted: 2016-02-25
• Last updated: 2019-09-27
• Results posted: 2019-09-27

Regulatory

• FDA-regulated device study