Clinical Trials Directory

Trials / Completed

CompletedNCT00762216

Rotational Stability of the AcrySof® Toric

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
71 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.

Conditions

Interventions

TypeNameDescription
DEVICEAcrySof® Toric intraocular lensImplantation of the AcrySof Toric intraocular lens (IOL) into the eye following cataract extraction surgery

Timeline

Start date
2008-05-01
Primary completion
2009-06-01
First posted
2008-09-30
Last updated
2012-10-31
Results posted
2010-05-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00762216. Inclusion in this directory is not an endorsement.

Rotational Stability of the AcrySof® Toric (NCT00762216) · Clinical Trials Directory