NCT00719732View on ClinicalTrials.gov

Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3

PHASE4CompletedINTERVENTIONAL
Enrollment

218

Participants

Timeline

Start Date

September 30, 2007

Primary Completion Date

May 31, 2009

Study Completion Date

May 31, 2009

Conditions
Cataract
Interventions
DEVICE

ReSTOR

Enrolled subjects receive implantation of ReSTOR +3 intraocular lenses (IOLs) for replacement of cataract in the natural lens of the eye. The patients were to be implanted bilaterally (in both eyes).

Trial Locations (1)

76134

Alcon Call Center for Trial Locations, Fort Worth

Sponsors

Lead Sponsor

Alcon Research
All Listed Sponsors
lead

Alcon Research

INDUSTRY