NCT00720005View on ClinicalTrials.gov

Evaluation of the Aspheric ReSTOR IOL After Routine Cataract Extraction

CompletedOBSERVATIONAL
Enrollment

20

Participants

Timeline

Start Date

September 30, 2007

Primary Completion Date

December 31, 2008

Study Completion Date

December 31, 2008

Conditions
Cataract
Interventions
DEVICE

Aspheric Acrysof ReSTOR intraocular lens

Bilateral implantation of Aspheric Acrysof ReSTOR

Trial Locations (1)

29425

Storm Eye Institute, Medical University of South Carolina, Charleston

All Listed Sponsors
lead

Medical University of South Carolina

OTHER

NCT00720005 - Evaluation of the Aspheric ReSTOR IOL After Routine Cataract Extraction | Biotech Hunter | Biotech Hunter