NCT01952665 - A Multi-Center Study Comparing the Clinical Performance of Two Silicone Hydrogel Lenses Over 1 Month of Daily Wear | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

November 30, 2013

Study Completion Date

March 31, 2014

Conditions

Myopia

Interventions

DEVICE

comfilcon A

Each subject randomized to wear the test lens (comfilcon A) or the control lens (lotrafilcon B) for one month of daily wear before repeating schedule for the second pair without a washout period.

DEVICE

lotrafilcon B

Each subject randomized to wear the test lens (comfilcon A) or the control lens (lotrafilcon B) for one month of daily wear before repeating schedule for the second pair without a washout period.

Trial Locations (6)

45701

Drs. Quinn, Foster, &Associates, Athens

55340

Complete Eye Care of Medina, Medina

60453

Davis EyeCare Associates, Oak Lawn

66762

Kannarr Eye Care LLC, Pittsburg

90606

Golden Optometric Group, Whittier

95008

Family Eye Care Center, Campbell

All Listed Sponsors

lead

CooperVision, Inc.

INDUSTRY