NCT01257217

A Comparison of Visual Function After Bilateral Implantation of Presbyopia-Correcting Intraocular Lenses (IOLs)

A Randomized, Subject-Masked Comparison of Visual Function After Bilateral Implantation of Presbyopia-Correcting IOLs

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 31 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 21 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to evaluate visual and refractive parameters in a series of subjects bilaterally implanted with presbyopia-correcting intraocular lenses (IOLs) during cataract surgery.

Detailed description

Each subject completed a preoperative examination of both eyes, implantation of IOL at the operative visit for each eye, and up to 4 postoperative visits (each eye examined at Day 1-2, with binocular visits at Month 1 and Month 3 after the second implantation). The second implantation occurred within 30 days of the first.

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	AcrySof® IQ ReSTOR® +3.0 D Multifocal IOL Model SN6AD1	Multifocal IOL implanted for long-term use over the lifetime of the cataract patient
DEVICE	AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric IOL Model SND1TT	Multifocal IOL with extended secondary focal point and astigmatism correction implanted for long-term use over the lifetime of the cataract patient
DEVICE	Acri.LISA® 366D IOL	Aspheric diffractive IOL with +3.75 D add power implanted for long-term use over the lifetime of the cataract patient
DEVICE	Acri.LISA® 466TD Toric IOL	Aspheric diffractive IOL with +3.75 D add power and astigmatism correction implanted for long-term use over the lifetime of the cataract patient

Timeline

• Start date: 2010-11-01
• Primary completion: 2011-06-01
• Completion: 2011-06-01
• First posted: 2010-12-09
• Last updated: 2018-07-02
• Results posted: 2017-04-20