NCT00838045View on ClinicalTrials.gov

Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular Lens

PHASE4CompletedINTERVENTIONAL
Enrollment

125

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

April 30, 2008

Study Completion Date

September 30, 2008

Conditions
CataractAphakia
Interventions
DEVICE

The Bausch & Lomb Akreos TL IOL (MI60) posterior chamber IOL

Surgery to implant the Bausch \& Lomb Akreos TL Intraocular Lens will be performed using standard microsurgical techniques following cataract surgery.

Trial Locations (1)

60590

Klinikum der J.W. Goethe-Universität, Frankfurt

All Listed Sponsors
lead

Bausch & Lomb Incorporated

INDUSTRY

NCT00838045 - Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular Lens | Biotech Hunter | Biotech Hunter