Comparison of ACUVUE® OASYS MAX 1-Day Multifocal and DAILIES® AquaComfort Plus® Multifocal

Part of paid clinical trials in Longwood, Florida.

Sponsor
Johnson & Johnson Vision Care, Inc.
Study ID
NCT07788521
Status
Not Yet Recruiting

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Conditions

  • Visual Acuity

Eligibility Criteria

Sex
ALL
Age
40 Years - 70 Years
Healthy Volunteers
Accepted

Interventions

  • Senofilcon A — DEVICE
    ACUVUE® Oasys MAX 1-Day Multifocal
  • Nelfilcon A — DEVICE
    DAILIES® AquaComfort Plus® Multifocal

Study Details

This study is a 4-visit, multi-site, prospective, controlled, randomized, single-masked (subjects), two-arm parallel group, bilateral, dispensing clinical trial to compare the performance of the Test lens to the Control lens in terms of safety and efficacy.

Key Dates

First listed
Aug 26, 2026
Start date
Aug 25, 2026
Status verified
Aug 2026
Primary completion
Dec 11, 2026
Completion
Dec 11, 2026

Study Design

Enrollment
150 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Senofilcon A
    Eligible subjects will be randomized to the Senofilcon A Lens for the duration of the study.
  • Active Comparator: Nelfilcon A
    Eligible subjects will be randomized to the Nelfilcon A Lens for the duration of the study.

Primary Outcome Measure

Mean binocular HLHC distance Visual Acuity [ Time Frame: At 1-week follow-up ]

Central Contacts

Locations (11)

FacilityCityStateZIPSite coordinators
Pearson Research Center PALongwoodFlorida32779-
VisualEyesRoswellGeorgia30076-
The Koetting AssociatesSt LouisMissouri63144-
Spectrum EyecareJamestownNew York14701-
Center for Ophthalmic and Vision Research/Eye Associates of New YorkManhattanNew York10022-
Sacco Eye GroupVestalNew York13850-
Dr. David W. Ferris & AssociatesWarwickRhode Island02888-
Total Eye CareMemphisTennessee38119-
Paradigm Research Center, LLCHoustonTexas77030-
Tyler Eye AssociatesTylerTexas75703-
Botetourt Eyecare, LLCSalemVirginia24153-

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