Clinical Trials Directory

Trials / Terminated

TerminatedNCT01241279

Accommodation Measurements After Bilateral Implantation of an Aspheric Accommodating Lens and Monofocal Aspheric Lenses

A Two Arm Prospective, Randomized, Double-Masked Clinical Evaluation of Accommodation Measurements After Bilateral Implantation of an Aspheric Accommodating Lens and Monofocal Aspheric Lenses

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

Summary

The objective of this study is to demonstrate the correlation of near vision and changes in higher order aberrations following lens extraction and to characterize the defocus curves of Crystalens® AO™ intraocular lens (IOL) versus the monofocal aspheric SofPort® LI61AO IOL in adults.

Conditions

Interventions

TypeNameDescription
DEVICECrystalens AOParticipants will undergo small incision cataract surgery (phacoemulsification). At the time of surgery, eligible participants will be implanted bilaterally with the Crystalens AO intraocular lens.
DEVICESoftPort LI61AOParticipants will undergo small incision cataract surgery (phacoemulsification). At the time of surgery, eligible participants will be implanted bilaterally with the SoftPort LI61AO intraocular lens.

Timeline

Start date
2010-10-01
Primary completion
2011-11-01
Completion
2011-12-01
First posted
2010-11-16
Last updated
2014-11-26
Results posted
2014-11-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01241279. Inclusion in this directory is not an endorsement.