ClinicalTrials.Veeva

Menu

Clinical Evaluation of a Reusable Multifocal Optical Design in a Presbyopic Population Phase 2

Johnson & Johnson (J&J) logo

Johnson & Johnson (J&J)

Status

Completed

Conditions

Visual Acuity

Treatments

Device: etafilcon A Sphere
Device: etafilcon A Multifocal
Device: senofilcon A Sphere
Device: senofilcon A Multifocal

Study type

Interventional

Funder types

Industry

Identifiers

NCT03586648
CR-6267

Details and patient eligibility

About

This is a single-masked, randomized-controlled, dispensing clinical trial. A total of approximately 60 eligible hyperopic subjects will be targeted to complete this study.

Enrollment

71 patients

Sex

All

Ages

40 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Potential subjects must satisfy all the following criteria to be enrolled in the study:

    1. The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form.

    2. The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.

    3. The subject must be between 40 and 70 years of age (inclusive).

    4. The subject's distance spherical equivalent refraction must be in the range of -1.25 D to -3.75 D in each eye.

    5. The subject's refractive cylinder must be ≤0.75 D in each eye.

    6. The subject's ADD power must be in the range of +0.75 D to +2.50 D.

    7. The subject must have distance best corrected visual acuity of 20/20-3 or better in each eye.

    8. Subjects must own a wearable pair of spectacles if required for their distance vision.

    9. The subject must be an adapted soft contact lens wearer in both eyes (i.e. worn lenses a minimum of 2 days per week for at least 8 hours per wear day, for 1 month of more duration).

    10. The subject must 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".

      Exclusion Criteria:

  • Potential subjects who meet any of the following criteria will be excluded from participating in the study:

    1. Currently pregnant or lactating.
    2. Any active or ongoing ocular or systemic allergies that may interfere with contact lens wear.
    3. 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).
    4. Clinically significant (Grade 3 or 4) corneal edema, corneal vascularization, corneal staining, tarsal abnormalities or bulbar injection, or any other corneal or ocular abnormalities which would contraindicate contact lens wear.
    5. Entropion, ectropion, extrusions, chalazia, recurrent styes, dry eye, glaucoma, history of recurrent corneal erosions.
    6. Any previous, or planned, ocular or intraocular surgery (e.g. radial keratotomy, PRK, LASIK, lid procedures, cataract surgery, retinal surgery, etc.).
    7. A history of amblyopia, strabismus or binocular vision abnormality.
    8. Any current ocular infection or inflammation.
    9. Any current ocular abnormality that may interfere with contact lens wear.
    10. Use of any of the following oral medications within 1 week prior to enrollment: oral retinoid isotretinoin (e.g. Accutane), oral tetracyclines, topical scopolamine, oral antihistamines (e.g., Chlor-Trimeton, and Benadryl), systemic steroids.
    11. Use of any ocular medication, with the exception of rewetting drops.
    12. History of herpetic keratitis.
    13. Participation in any contact lens or lens care product clinical trial within 30 days prior to study enrollment.
    14. Employee or immediate family member of an employee of clinical site (e.g., Investigator, Coordinator, Technician).
    15. Any known hypersensitivity or allergic reaction to Optifree®Replenish® multipurpose care solution or Eye-Cept® rewetting drop solution.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

71 participants in 2 patient groups

Test/Control
Experimental group
Description:
Hyperopic subjects who are habitual soft contact lens wearers between the ages of 40 and 70 years of age, will be randomized to sequence Test/Control. Alternative Spherical lenses will be used if optimization cannot be achieved with the Multifocal lenses.
Treatment:
Device: senofilcon A Multifocal
Device: senofilcon A Sphere
Device: etafilcon A Multifocal
Device: etafilcon A Sphere
Control/Test
Experimental group
Description:
Hyperopic subjects who are habitual soft contact lens wearers between the ages of 40 and 70 years of age, will be randomized to sequence Control/Test. Alternative Spherical lenses will be used if optimization cannot be achieved with the Multifocal lenses.
Treatment:
Device: senofilcon A Multifocal
Device: senofilcon A Sphere
Device: etafilcon A Multifocal
Device: etafilcon A Sphere

Trial documents
1

Trial contacts and locations

6

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems