Evaluation of Comfort for Two Marketed Daily Disposable Contact Lenses

Completed · Not applicable

Conditions studied: Visual Acuity

In brief

This study is a 2-phase adaptive approach utilizing a 2×2 crossover design. The study lenses will be worn in a bilateral fashion for a period of approximately 1-week each.

Key facts

Study ID

NCT04968925

Run by

Johnson & Johnson Vision Care, Inc.

People needed

302

Starts

2021-07-12

Expected to finish

2021-10-25

Last updated by the study team

2022-12-22

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Potential subjects must satisfy all of the following criteria to be enrolled in the study:
• Read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form.
• Appear able and willing to adhere to the instructions set forth in this clinical protocol.
• Be between 18 and 40 (inclusive) years of age at the time of screening.
• By self-report, habitually wear soft spherical contact lenses in both eyes in a daily disposable wear modality. Habitual wear is defined as a minimum of 8 hours of wear per day, for a minimum of 4 days per week during the past 4 weeks.
• By self-report, typically uses computer screens and other digital devices (phones, tablets) at least 30 hours per week.
• The vertex-corrected best spherical distance refraction (rounded to nearest 0.25 D) must be between -1.00 and -4.00 DS (inclusive) in each eye.
• The magnitude of the cylinder component of the subject's distance refraction must be 1.00 DC or less.
• The subject must have best corrected visual acuity of 20/25 or better in each eye.

You may not qualify if…

• Potential subjects who meet any of the following criteria will be excluded from participating in the study:
• Be currently pregnant or breastfeeding
• By self-report, have any ocular or systemic disease, allergies, infection, or use of medication that might contraindicate or interfere with contact lens wear, or otherwise compromise study endpoints, including infectious disease (e.g., hepatitis, tuberculosis), contagious immunosuppressive disease (e.g., Human Immunodeficiency Virus [HIV]), autoimmune disease (e.g. rheumatoid arthritis, Sjögren's syndrome), or history of serious mental illness or seizures. See Section 9.1 for additional details regarding excluded systemic medications.
• Have had any previous ocular or intraocular surgery (e.g., radial keratotomy, PRK, LASIK, cataract, etc.).
• Habitually wear monovision, multifocal, toric, or extended wear contact lens correction
• Have participated in any contact lens or lens care product clinical trial within 14 days prior to study enrollment
• Be an employee or immediate family member of an employee of clinical site (e.g., Investigator, Coordinator, Technician)
• Have a history of amblyopia or strabismus.
• Have habitually worn rigid gas permeable (RGP) lenses, orthokeratology lenses, or hybrid lenses (eg, SynergEyes) within the past 6 months.
• Have clinically significant (Grade 3 or higher on the FDA grading scale) slit lamp findings (e.g., corneal edema, neovascularization or staining, tarsal abnormalities or bulbar injection) or other corneal or ocular disease or abnormalities that contraindicate contact lens wear or may otherwise compromise study endpoints (including entropion, ectropion, chalazia, recurrent styes, glaucoma, history of recurrent corneal erosions, aphakia, moderate or above corneal distortion, herpetic keratitis).
• Have any ocular infection.

Where it is running

• James R. Dugue Optometry — Mission Viejo, California, United States
• Maitland Vision Center — Maitland, Florida, United States
• Flora Chen Poveda, OD, PA — Orange Park, Florida, United States
• Visual Eyes, Inc — Roswell, Georgia, United States
• VisionPoint Center — Bloomington, Illinois, United States
• ABQ Eye Care — Albuquerque, New Mexico, United States
• ProCare Vision Center — Granville, Ohio, United States
• Optometry Group LLC — Memphis, Tennessee, United States
• Gulf Coast Vision Center, Inc. — Houston, Texas, United States
• Tyler Eye Associates — Tyler, Texas, United States

Full record on ClinicalTrials.gov

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