Clinical Trials Directory

Trials / Completed

CompletedNCT00967473

ACRYSOF® Toric NATURAL T9 Intraocular Lens (IOL)

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

Summary

The purpose of this study is to describe rates of spatial distortions related to intraocular lens (IOL) misalignment for ACRYSOF® Single-Piece Toric NATURAL IOL Model SN60T9 when implanted bilaterally into the capsular bag following phacoemulsification in adult patients with bilateral cataract and regular corneal astigmatism. Subjects were implanted with the Model SN60T9 in the first operative (study) eye and either Model SN60T9 or Model SN60T8 in the second operative eye.

Conditions

Interventions

TypeNameDescription
DEVICEACRYSOF® Single-Piece NATURAL Toric IOL Model SN60T9 and Model SN60T8.ACRYSOF® Single-Piece Toric NATURAL Intraocular Lens (IOL) Model SN60T9 in the first eye and either the ACRYSOF® Single-Piece Toric NATURAL IOL Model SN60T9 or Model SN60T8 in the second eye.

Timeline

Start date
2009-08-01
Primary completion
2010-05-01
Completion
2010-05-01
First posted
2009-08-27
Last updated
2017-01-09
Results posted
2011-07-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00967473. Inclusion in this directory is not an endorsement.