Contact Lenses for Visual Acuity
What You Need to Know Before You Apply
What is the purpose of this trial?
This is a prospective, multi-site, bilateral, 2-week dispensing, randomized, controlled, single-masked (subjects), 2x2 crossover study to evaluate visual acuity.
Who Is on the Research Team?
Johnson & Johnson Vision Care, Inc. Clinical Trial
Principal Investigator
Johnson & Johnson Vision Care, Inc.
Are You a Good Fit for This Trial?
This trial is for people who need contact lenses and want to help test how well two different approved types work for vision. Participants must be able to wear contacts in both eyes and follow study instructions.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Trial Overview
The study compares two types of soft contact lenses—Serafilcon A (control) and Senofilcon A (test)—to see which provides better vision. Each person tries both lens types over separate 2-week periods, with the order chosen at random.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Eligible subjects will be randomized to the Test/Control sequence, to wear the Test Lens for approximately 2 weeks, undergo a 2-week washout period, and then wear the Control lens for approximately 2 weeks.
Eligible subjects will be randomized to the Control/Test sequence, to wear the Control Lens for approximately 2 weeks, undergo a 2-week washout period, and then wear the Test lens for approximately 2 weeks.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Johnson & Johnson Vision Care, Inc.
Lead Sponsor
Joaquin Duato
Johnson & Johnson Vision Care, Inc.
Chief Executive Officer since 2022
MBA from ESADE, Master of International Management from Thunderbird School of Global Management
Dr. Jijo James, MD
Johnson & Johnson Vision Care, Inc.
Chief Medical Officer since 2014
MD from St. Johns Medical College, MPH from Columbia University
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