NCT01449526View on ClinicalTrials.gov

A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design

NACompletedINTERVENTIONAL
Enrollment

166

Participants

Timeline

Start Date

August 31, 2011

Primary Completion Date

December 31, 2011

Study Completion Date

January 31, 2012

Conditions
Myopia
Interventions
DEVICE

B&L Investigational Contact Lens

Lenses will be worn on a daily wear basis for 3 months, new lenses dispensed monthly.

DEVICE

B&L PureVision Contact Lens

Lenses will be worn on a daily wear basis for 3 months, new lenses dispensed monthly.

All Listed Sponsors
lead

Bausch & Lomb Incorporated

INDUSTRY

NCT01449526 - A Study to Evaluate the Safety and Efficacy of a New Silicone Hydrogel Contact Lens Design | Biotech Hunter | Biotech Hunter