Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses

Last updated: September 22, 2025
Sponsor: Alcon Research
Overall Status: Completed

Phase

N/A

Condition

Eye Disorders/infections

Myopia

Presbyopia

Treatment

Senofilcon A multifocal contact lenses

Serafilcon A multifocal contact lenses

CLEAR CARE® Cleaning & Disinfecting Solution

Clinical Study ID

NCT06469242
CLM234-C001
  • Ages > 40
  • All Genders

Study Summary

The purpose of this study is to evaluate the on-eye multifocal clinical performance of investigational LID233309 contact lenses and Oasys multifocal (MF) contact lenses in a daily wear dispensing trial.

Eligibility Criteria

Inclusion

Key Inclusion Criteria:

  • Current wearer of biweekly/monthly replacement multifocal soft contact lenses inboth eyes for a minimum of 5 days per week and 10 hours per day during the past 6months.

  • Manifest cylinder equal to or less than 0.75 diopter (D) in each eye.

  • Able to wear contact lenses within the available power range with a near ADD of +0.75 D to +2.50 D in each eye.

  • Other protocol-defined inclusion criteria may apply.

Exclusion

Key Exclusion Criteria:

  • Currently pregnant or lactating.

  • History of amblyopia, strabismus, or binocular vision abnormalities.

  • Habitual Oasys MF contact lens wearers or daily disposable contact lens wearers.

  • Monovision contact lens wearers and wearers of contact lens in one eye only.

  • Other protocol-defined exclusion criteria may apply.

Study Design

Total Participants: 106
Treatment Group(s): 3
Primary Treatment: Senofilcon A multifocal contact lenses
Phase:
Study Start date:
July 18, 2024
Estimated Completion Date:
October 08, 2024

Study Description

Subjects will wear two different contact lens study products in a cross-over fashion. Each study product type will be worn for approximately 14 days. A washout period of 2-4 days will occur prior to the first wear period and between the two wear periods. Subjects will be expected to attend 7 office visits. The total duration of study participation is approximately 40 days with approximately 28 days of lens wear.

Connect with a study center

  • Kurata Eyecare Center

    Los Angeles, California 90013
    United States

    Site Not Available

  • Elsa Pao, OD

    Oakland, California 94607
    United States

    Site Not Available

  • Kurata Eyecare Center

    Los Angeles 5368361, California 5332921 90013
    United States

    Site Not Available

  • Elsa Pao, OD

    Oakland 5378538, California 5332921 94607
    United States

    Site Not Available

  • Drs. Giedd, P.A.

    Maitland, Florida 32751
    United States

    Site Not Available

  • Vision Health Institute

    Orlando, Florida 32803
    United States

    Site Not Available

  • Drs. Giedd, P.A.

    Maitland 4163220, Florida 4155751 32751
    United States

    Site Not Available

  • Vision Health Institute

    Orlando 4167147, Florida 4155751 32803
    United States

    Site Not Available

  • Wesley Optometric Consulting

    Medina, Minnesota 55340
    United States

    Site Not Available

  • Wesley Optometric Consulting

    Medina 5037186, Minnesota 5037779 55340
    United States

    Site Not Available

  • ProCare Vision Centers, Inc.

    Granville, Ohio 43023
    United States

    Site Not Available

  • Insight Research Clinic LLC

    Powell, Ohio 43065
    United States

    Site Not Available

  • ProCare Vision Centers, Inc.

    Granville 5156270, Ohio 5165418 43023
    United States

    Site Not Available

  • Insight Research Clinic LLC

    Powell 5167350, Ohio 5165418 43065
    United States

    Site Not Available

  • Optometry Group, PLLC

    Memphis, Tennessee 38111
    United States

    Site Not Available

  • Optometry Group, PLLC

    Memphis 4641239, Tennessee 4662168 38111
    United States

    Site Not Available

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