NCT01299155

A Comparison of Visual Function After Bilateral Implantation of Presbyopia Correcting Intraocular Lenses

A Randomized, Pilot Study, Subject Masked Comparison of Visual Function After Bilateral Implantation of Presbyopia Correcting Intraocular Lenses (IOLs)

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 24 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 21 Years
• Healthy volunteers: Not accepted

Summary

To prospectively evaluate postoperative visual and refractive parameters in a series of subjects bilaterally implanted with AcrySof ReSTOR +3 vs. those bilaterally implanted with LENTIS MPlus Intraocular Lens (IOL).

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	ReSTOR +3	Bilateral implantation of an Alcon AcrySof ReSTOR +3 Intraocular Lens (IOL) Model SN6AD1 following cataract extraction.
DEVICE	LENTIS MPlus	Bilateral implantation of a LENTIS MPlus Intraocular Lens (IOL) following cataract extraction.

Timeline

• Start date: 2011-03-01
• Primary completion: 2011-09-01
• First posted: 2011-02-18
• Last updated: 2012-10-23

Locations

1 site across 1 country: Spain