Comparison of a Daily Disposable Multifocal Contact Lens to a Marketed Product

Completed · Not applicable

Conditions studied: Visual Acuity

In brief

This is a single-masked, two-arm, parallel-group, randomized-controlled, dispensing clinical trial to evaluate the visual performance.

Key facts

Study ID

NCT05101252

Run by

Johnson & Johnson Vision Care, Inc.

People needed

77

Starts

2021-10-11

Expected to finish

2021-11-29

Last updated by the study team

2023-01-10

Who can join

Age: 40 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Potential subjects must satisfy all 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 at least 40 years of age and not greater than 70 years of age at the time of consent.
• Own a wearable pair of spectacles if required for their distance vision.
• Be an adapted soft contact lens wearer in both eyes (i.e. worn lenses a minimum of 2 days per week for at least 6 hours per wear day, for 1 month or more duration).
• Either already be wearing a presbyopic contact lens correction (e.g., reading spectacles over contact lenses, multifocal or monovision contact lenses, etc.) or if not respond positively to at least one symptom on the "Presbyopic Symptoms Questionnaire".
• The subject's distance spherical equivalent refraction must be in the range of -1.25 D to -3.75 D or +1.25 D to +3.75 D in each eye.
• The subject's refractive cylinder must be ≤0.75 D in each eye.
• The subject's ADD power must be in the range of +0.75 D to +2.50 D.
• The subject must have distance best corrected visual acuity of 20/20-3 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 lactating.
• Have any active or ongoing ocular or systemic allergies that may interfere with contact lens wear.
• Have any active or ongoing systemic disease, autoimmune disease, or use of medication, which may interfere with contact lens wear. This may include, but not be limited to, diabetes, hyperthyroidism, Sjögren's syndrome, xerophthalmia, acne rosacea, Stevens-Johnson syndrome, and immunosuppressive diseases or any infectious diseases (e.g. hepatitis, tuberculosis).
• Have any previous, or planned, ocular or intraocular surgery (e.g. radial keratotomy, PRK, LASIK, lid procedures, cataract surgery, retinal surgery, etc.).
• Have a history of amblyopia, strabismus or binocular vision abnormality.
• Use of any of the following medications within 1 week prior to enrollment: oral retinoid, oral tetracyclines, anticholinergics, oral phenothiazines, oral/inhaled corticosteroids. See Table 9.1 for further examples.
• Use of any ocular medication, with the exception of rewetting drops.
• Have a history of herpetic keratitis.
• Have a history of irregular cornea.
• Have a history of pathological dry eye.
• Have Participated in any contact lens or lens care product clinical trial within 30 days prior to study enrollment.
• Be and employee or immediate family member of an employee of clinical site (e.g., Investigator, Coordinator, Technician).
• Have any known hypersensitivity or allergic reaction to non-preserved rewetting drop solutions or sodium fluorescein.
• Have clinically significant (Grade 3 or greater) corneal edema, corneal vascularization, corneal staining, tarsal abnormalities or bulbar injection, or any other corneal or ocular abnormalities which would contraindicate contact lens wear.
• Have any current ocular infection or inflammation.
• Have any current ocular abnormality that may interfere with contact lens wear.

Where it is running

• Stam & Associates Eye Care — Jacksonville, Florida, United States
• Sabal Eye Care — Longwood, Florida, United States
• Visual Eyes — Roswell, Georgia, United States
• Kannarr Eye Care — Pittsburg, Kansas, United States
• Birmingham Vision Care — Bloomfield Township, Michigan, United States
• Eye Associates of New York — New York, New York, United States
• ProCare Vision Centers — Granville, Ohio, United States
• West Bay Eye Associates — Warwick, Rhode Island, United States
• Tyler Eye Associates — Tyler, Texas, United States

Full record on ClinicalTrials.gov

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