NCT01122576

Evaluation of 3 Intraocular Lenses Following Lens Extraction

A Three Arm Prospective Clinical Evaluation of Three FDA Approved Intraocular Lenses Designed to Improve Distance, Intermediate and Near Vision Following Lens Extraction.

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 78 (actual)
• Sponsor: Bausch & Lomb Incorporated · Industry
• Sex: All
• Age: 40 Years
• Healthy volunteers: Not accepted

Summary

The objective of this study is to evaluate the efficacy and subject satisfaction with three different FDA approved lenses for adults over 40 years of age who desire a reduction in spectacle dependence.

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	Crystalens AO	Crystalens AO surgically implanted bilaterally. Study observation up to 180 days.
DEVICE	ReSTOR	ReSTOR surgically implanted bilaterally. Study observation up to 180 days.
DEVICE	Tecnis Multifocal IOL	Tecnis surgically implanted bilaterally. Study observation up to 180 days.

Timeline

• Start date: 2010-06-01
• Primary completion: 2012-06-01
• Completion: 2012-09-01
• First posted: 2010-05-13
• Last updated: 2014-03-28
• Results posted: 2014-03-28

Locations

1 site across 1 country: United States