NCT00733512View on ClinicalTrials.gov

Surgeon Experience ReSTOR A +4 Intraocular Lens (IOL)

CompletedOBSERVATIONAL
Enrollment

146

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

March 31, 2008

Study Completion Date

March 31, 2008

Conditions
Cataract
Interventions
DEVICE

ReSTOR

Patients were implanted with the AcrySof ReSTOR Aspheric +4 Intraocular Lens (IOL) in one or both eyes for treatment of cataract.

Trial Locations (1)

76134

Alcon Call Center for Trial Locations, Fort Worth

Sponsors

Lead Sponsor

Alcon Research
All Listed Sponsors
lead

Alcon Research

INDUSTRY