Evaluation of Approved Contact Lenses (CR-6657)

Part of paid clinical trials in Jacksonville, Florida.

Sponsor
Johnson & Johnson Vision Care, Inc.
Study ID
NCT07819305
Status
Not Yet Recruiting

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Conditions

  • Visual Acuity

Eligibility Criteria

Sex
ALL
Age
18 Years - 39 Years
Healthy Volunteers
Accepted

Interventions

  • Test (Senofilcon A) — DEVICE
    Test Lens
  • Control (Serafilcon A) — DEVICE
    Precision7®

Study Details

This is a prospective, multi-site, bilateral, 2-week dispensing, randomized, controlled, single-masked (subjects), 2x2 crossover study to evaluate visual acuity.

Key Dates

First listed
Sep 14, 2026
Start date
Sep 10, 2026
Status verified
Sep 2026
Primary completion
Dec 3, 2026
Completion
Dec 3, 2026

Study Design

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

Arms

  • Experimental: Test/Control
    Eligible subjects will be randomized to the Test/Control sequence, to wear the Test Lens for approximately 2 weeks, undergo a 2-week washout period, and then wear the Control lens for approximately 2 weeks.
  • Experimental: Control/Test
    Eligible subjects will be randomized to the Control/Test sequence, to wear the Control Lens for approximately 2 weeks, undergo a 2-week washout period, and then wear the Test lens for approximately 2 weeks.

Primary Outcome Measure

Binocular High Luminance, Low Contrast (HLLC) Distance (4 meters) Visual Acuity (logMAR) at 2-week Follow-up [ Time Frame: At 2-week follow-up ]

Central Contacts

Locations (8)

FacilityCityStateZIPSite coordinators
VRCJacksonvilleFlorida32256-
Franklin Park Eye Center, P.C.Franklin ParkIllinois60131-
Eyecare Center of CamdenCamdenNew York13316-
ProCare Vision CentersGranvilleOhio43023-
New Bremen EyeCareNew BremenOhio45869-
Total Eye CareMemphisTennessee38119-
Paradigm Research Center, LLCHoustonTexas77030-
Botetourt Eyecare, LLCSalemVirginia24153-

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