A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses

NACompletedINTERVENTIONAL
Enrollment

216

Participants

Timeline

Start Date

April 30, 2012

Primary Completion Date

June 30, 2012

Study Completion Date

July 31, 2012

Conditions
Myopia
Interventions
DEVICE

B&L RD2135-01 lens C

Lenses will be worn on a daily wear basis for 1 week. Lens care solution and lens cases will be provided for daily rinsing, cleaning, disinfecting, and storing the lenses. Rewetting drops will be provided for use as needed during the study.

DEVICE

B&L RD2135-01 lens D

Lenses will be worn on a daily wear basis for 1 week. Lens care solution and lens cases will be provided for daily rinsing, cleaning, disinfecting, and storing the lenses. Rewetting drops will be provided for use as needed during the study.

DEVICE

PureVision2

Lenses will be worn on a daily wear basis for 1 week. Lens care solution and lens cases will be provided for daily rinsing, cleaning, disinfecting, and storing the lenses. Rewetting drops will be provided for use as needed during the study.

DEVICE

Air Optix Aqua

Lenses will be worn on a daily wear basis for 1 week. Lens care solution and lens cases will be provided for daily rinsing, cleaning, disinfecting, and storing the lenses. Rewetting drops will be provided for use as needed during the study.

Trial Locations (1)

14609

Bausch & Lomb Incorporated, Rochester

All Listed Sponsors
lead

Bausch & Lomb Incorporated

INDUSTRY

NCT01583868 - A Study to Evaluate the Product Feasibility of Two New Silicone Hydrogel Contact Lenses | Biotech Hunter | Biotech Hunter