Evaluation of Approved Contact Lenses
Not Applicable
Not yet recruiting
- Conditions
- Visual Acuity
- Registration Number
- NCT07174596
- Lead Sponsor
- Johnson & Johnson Vision Care, Inc.
- Brief Summary
This is a prospective, randomized, controlled, subject-masked, bilateral, dispensing, multi-site, 2 lenses × 3 wearing periods crossover study to evaluate visual acuity.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 88
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Proportion of Eyes Achieving 20/20 Distance Monocular Snellen VA or Better at the 1-week follow-up visit At 1-week follow-up per wear period Visual acuity (VA) will be collected for each eye at distance using Snellen charts at the fitting evaluation and after approximately 1-week of lens wear.
Proportion of Eyes with acceptable lens fit Up to 3-week follow-up Acceptable lens fit will be assessed at all study visits (scheduled and unscheduled) for each eye.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (4)
VisualEyes
🇺🇸Roswell, Georgia, United States
New Bremen EyeCare
🇺🇸New Bremen, Ohio, United States
Botetourt Eyecare LLC
🇺🇸Salem, Virginia, United States
New River Vision Care
🇺🇸Oak Hill, West Virginia, United States
VisualEyes🇺🇸Roswell, Georgia, United States